Article 1DefinitionsFor the purposes of this Directive, the following terms shall have the following meanings:(a)vessel: any vessel flying the flag of a Member State or registered under the plenary jurisdiction of a Member State, seagoing or estuary-fishing, publicly or privately owned, excluding:inland navigation vessels,warships,pleasure boats used for non-commercial purposes and not manned by professional crews,tugs operating in harbour areas.Vessels shall be classed in three categories in accordance with Annex I;(b)worker: any person carrying out an occupation on board a vessel, including trainees and apprentices, but excluding port pilots and shore personnel carrying out work on board a vessel at the quayside;(c)Owner: the registered owner of a vessel unless that vessel has been chartered by demise or is managed, either wholly or in part, by a natural or legal person other than the registered owner under the terms of a management agreement; in that case the owner shall be construed as the demise charterer or natural or legal person managing the vessel as appropriate;(d)medical supplies: medicines, medical equipment and antidotes, a non-exhaustive list of which is given in Annex II;(e)antidote: a substance used to prevent or treat a harmful effect or effects, direct or indirect, of one or more substances included on the list of dangerous substances in Annex III.

Article 2Medicines and medical equipment — Sick-bay — DoctorEach Member State shall take the measures necessary to ensure that:1.(a)every vessel flying its flag or registered under its plenary jurisdiction always carries on board medical supplies which meet at least, in terms of quality, the specifications of Annex II sections I and II for the category of vessel to which it belongs;(b)the quantities of medicinal products and medical equipment to be carried depend on the nature of the voyage — in particular ports of call, destination, duration — the type or types of work to be carried out during the voyage, the nature of the cargo and the number of workers;(c)the content of the medicines and medical equipment included in the medical supplies shall be detailed on a checklist corresponding at least to the general framework laid down in Annex IV, sections A, B and C II 1 and II 2;2.(a)for each of its life-rafts and life-boats, every vessel flying its flag or registered under its plenary jurisdiction carries a watertight medicine chest at least containing the medical supplies specified in Annex II, sections I and II, for category C vessels;(b)the content of these chests is also detailed on the checklist referred to in paragraph 1 (c);3.every vessel flying its flag or registered under its plenary jurisdiction, of more than 500 gross registered tonnes, with a crew of 15 or more workers and engaged on a voyage of more than three days, has a sick-bay in which medical treatment can be administered under satisfactory material and hygienic conditions;4.every vessel flying its flag or registered under its plenary jurisdiction, with a crew of 100 or more workers and engaged on an international voyage of more than three days, has a doctor responsible for the medical care of the workers on board.

Article 3AntidotesEach Member State shall take the measures necessary to ensure that:1.any vessel flying its flag or registered under its plenary jurisdiction and carrying any of the dangerous substances listed in Annex III carries on board medical supplies including at least the antidotes listed in Section III of Annex II;2.any ferry-type vessels flying its flag or registered under its plenary jurisdiction, whose conditions of operation do not always allow it to know well enough in advance the nature of the dangerous substances being transported, has on board medical supplies including at least the antidotes listed in section III of Annex II.However, on a regular where the crossing is due to last less than two hours, the antidotes may be limited to those which have to be administered in cases of extreme emergency within a period of time not exceeding the normal duration of the crossing;3.the contents of the medical supplies, as regards antidotes, shall be detailed on a check list corresponding at least to the general framework laid down in Annex IV, sections A, B and C, II 3.

Article 4Allocation of responsibilitiesEach Member State shall take the measures necessary to ensure that:1.(a)the provision and replenishment of the medical supplies of any vessel flying its flag or registered under its plenary jurisdiction are undertaken on the exclusive responsibility of the owner, without any expense to the workers;(b)the management of the medical supplies is placed under the responsibility of the captain of the vessel; he may, without prejudice to this responsibility, delegate the use and maintenance of the medical supplies to one or more workers specially designated by reason of their competence;2.the medical supplies are maintained in good condition and replenished and/or replaced as soon as possible, and in every case as a priority part of normal revictualling procedures;3.in an emergency established by the captain as far as possible after having obtained a medical opinion, the required medicines, medical equipment and antidotes which are not available on board are made available as soon as possible.

Article 5Information and trainingEach Member State shall take the measures necessary to ensure that:1.medical supplies are accompanied by one or more guides to their use, including instructions for use of at least the antidotes required in Annex II section III;2.all persons receiving professional maritime training and intending to work on board ship have been given basic training in the medical and emergency measures to be taken immediately in the event of an accident or serious medical emergency;3.the captain and any worker or workers to whom he delegates the use of the medical supplies pursuant to Article 4 (1) (b) have received special training updated periodically, at least every five years, taking into account the specific risks and needs connected with the different categories of vessel and in accordance with the general guidelines set out in Annex V.

Article 6Medical consultations by radio1.To ensure better emergency treatment for workers, each Member State shall take the measures necessary to ensure that:(a)one or more centres are designated to provide workers with free medical advice by radio;(b)some of the doctors providing their services for the radio consultation centres have been trained in the special conditions prevailing on board ship.2.In order to optimize the advice given, the radio consultation centres may keep personal medical records, with the agreement of the workers concerned.Such records shall remain confidential.

Article 7Inspection1.Each Member State shall take the measures necessary to ensure that a competent person or a competent authority carries out an annual inspection to check that on board all vessels flying its flag:the medical supplies meet the minimum requirements of this Directive;the checklist provided for in Article 2 (1) (c) confirms that the medical supplies comply with those minimum requirements;the medical supplies are correctly stored;any expiry dates have been respected.2.Inspections of the medical supplies stored on life-rafts shall be carried out in the course of those life-rafts' annual maintenance.Those inspections may exceptionally be postponed for up to five months.

Article 8Amendments to the AnnexesThe Commission is empowered to adopt delegated acts in accordance with Article 8a to make strictly technical amendments to the Annexes, in order to take account of technical progress or changes in international regulations or specifications and new findings concerning medical treatment on board vessels.Where, in duly justified and exceptional cases involving imminent, direct and serious risks to workers’ and other persons’ physical health and safety, imperative grounds of urgency require action in a very short timeframe, the procedure provided for in Article 8b shall apply to delegated acts adopted pursuant to this Article.

Article 8aExercise of the delegation1.The power to adopt delegated acts is conferred on the Commission subject to the conditions laid down in this Article.2.The power to adopt delegated acts referred to in Article 8 shall be conferred on the Commission for a period of five years from 26 July 2019. The Commission shall draw up a report in respect of the delegation of power not later than nine months before the end of the five-year period. The delegation of power shall be tacitly extended for periods of an identical duration, unless the European Parliament or the Council opposes such extension not later than three months before the end of each period.3.The delegation of power referred to in Article 8 may be revoked at any time by the European Parliament or by the Council. A decision to revoke shall put an end to the delegation of the power specified in that decision. It shall take effect the day following the publication of the decision in the Official Journal of the European Union or at a later date specified therein. It shall not affect the validity of any delegated acts already in force.4.Before adopting a delegated act, the Commission shall consult experts designated by each Member State in accordance with the principles laid down in the Interinstitutional Agreement of 13 April 2016 on Better Law-MakingOJ L 123, 12.5.2016, p. 1..5.As soon as it adopts a delegated act, the Commission shall notify it simultaneously to the European Parliament and to the Council.6.A delegated act adopted pursuant to Article 8 shall enter into force only if no objection has been expressed either by the European Parliament or the Council within a period of two months of notification of that act to the European Parliament and the Council or if, before the expiry of that period, the European Parliament and the Council have both informed the Commission that they will not object. That period shall be extended by two months at the initiative of the European Parliament or of the Council.

Article 8bUrgency procedure1.Delegated acts adopted under this Article shall enter into force without delay and shall apply as long as no objection is expressed in accordance with paragraph 2. The notification of a delegated act to the European Parliament and the Council shall state the reasons for the use of the urgency procedure.2.Either the European Parliament or the Council may object to a delegated act in accordance with the procedure referred to in Article 8a(6). In such a case, the Commission shall repeal the act immediately following the notification of the decision to object by the European Parliament or by the Council.

Article 9Final provisions1.Member States shall bring into force the laws, regulations and administrative provisions necessary to comply with this Directive by 31 December 1994. They shall forthwith inform the Commission thereof.When Member States adopt these measures, such measures shall contain a reference to this Directive or shall be accompanied by such reference on the occasion of their official publication. The methods of making such a reference shall be laid down by the Member States.2.Member States shall communicate to the Commission the texts of the provisions of national law which they have already adopted or which they adopt in the field governed by this Directive.3.Member States shall report to the Commission every five years on the implementation of this Directive, giving the views of the two sides of industry.The Commission shall inform the European Parliament, the Council, the Economic and Social Committee and the Advisory Committee for Safety, Hygiene and Health at Work thereof.4.The Commission shall report at least every five years to the European Parliament, the Council and the Economic and Social Committee on the implementation of this Directive, taking into account paragraphs 1, 2 and 3.

Article 9aImplementation reportEvery five years, the Member States shall submit to the Commission a report on the practical implementation of this Directive in the form of a specific chapter of the single report referred to in Article 17a(1), (2) and (3) of Directive 89/391/EEC, which serves as a basis for the Commission’s evaluation, in accordance with Article 17a(4) of that Directive..

Article 10This Directive is addressed to the Member States.

nullANNEX ICATEGORIES OF VESSELS(Article 1 (a))A.Sea-going or sea-fishing vessels, with no limitation on length of trips.B.Sea-going or sea-fishing vessels making trips of less than 150 nautical miles from the nearest port with adequate medical equipmentCategory B shall be extended to sea-going or sea-fishing vessels which make trips of less than 175 nautical miles from the nearest port with adequate medical equipment and which remain continuously within range of helicopter rescue services.To this end, each Member State shall forward up-to-date information on the areas in which routine helicopter rescue services are provided, and the circumstances in which they operate:(a)to the other Member States and the Commission; and(b)to the captains of vessels flying its flag or registered under its plenary jurisdiction who are, or are likely to be, concerned by application of the first subparagraph of this footnote; the information shall be forwarded in the most appropriate way, for example through radio-consultation centres, rescue coordination centres or coastal radio stations..C.Harbour vessels, boats and craft staying very close to shore or with no cabin accommodation other than a wheelhouse.ANNEX IIMEDICAL SUPPLIES (NON-EXHAUSTIVE LIST)(Article 1 (d))I.MEDICINES

1.Cardiovascular2.Gastro-intestinal system3.Analgesics and anti-spasmodics4.Nervous system5.Anti-allergics and anti-anaphylactics6.Respiratory system7.Anti-infection9.Medicines for external use(a)Skin medicines(b)Eye medicines(c)Ear medicines(d)Medicines for oral and throat infections(e)Local anaesthetics

	A	B	C
	Categories of vessels
(a)Cardio-circulatory analeptics — Sympathomimetics	×	×
(b)Anti-angina preparations	×	×	×
(c)Diuretics	×	×
(d)Anti-haemorrhagics including uterotonics if there are women on board	×	×	×
(e)Anti-hypertensive	×
(a)Medicines for gastric and duodenal disorders
—Histamine H2 receptor anti-ulcer antagonists	×
—Anti-acid mucous dressings	×	×
(b)Anti-emetics	×	×	×
(c)Lubricant laxatives	×
(d)Anti-diarrhoeals	×	×	×
(e)Intestinal antiseptics	×	×
(f)Haemorrhoid preparations	×	×
(a)Analgesics, anti-pyretics and anti-inflammatory preparations	×	×	×
(b)Powerful analgesics	×	×
(c)Spasmolytics	×	×
(a)Anxiolytics	×	×
(b)Neuroleptics	×	×
(c)Seasickness remedies	×	×	×
(d)Anti-epileptics	×
(a)H1 Anti-histaminics	×	×
(b)Injectable glucocorticoids	×	×
(a)Bronchiospasm preparations	×	×
(b)Anti-tussives	×	×
(c)Medicines used for colds and sinusitis	×	×
(a)Antibiotics (at least two families)	×	×
(b)Anti-bacterial sulphamide	×	×
(c)Urinary antiseptics	×
(d)Anti-parasitics	×	×
(e)Intestinal anti-infectives	×	×
(f)Anti-tetanus vaccines and immunoglobulins	×	×
8.Compounds promoting rehydration, caloric intake and plasma expansion	×	×
—Antiseptic solutions	×	×	×
—Antibiotic ointments	×	×
—Anti-inflammatory and analgesic ointments	×	×
—Anti-mycotic skin creams	×
—Burn preparations	×	×	×
—Antibiotic drops	×	×
—Antibiotic and anti-inflammatory drops	×	×
—Anaesthetic drops	×	×
—Hypotonic myotic drops	×	×
—Antibiotic solutions	×	×
—Anaesthetic and anti-inflammatory solutions	×	×
—Antibiotic or antiseptic mouthwashes	×	×
—Local anaesthetics using freezing	×
—Local anaesthetics given by subcutaneous injection	×	×
—Dental anaesthetic and antiseptic mixtures	×	×

II.MEDICAL EQUIPMENT

Under the conditions of use prescribed by national laws and/or practices.1.Resuscitation equipment2.Dressing and suturing equipment3.Instruments4.Examination and monitoring equipment5.Equipment for injection, perfusion, puncture and catheterization6.General medical equipment7.Immobilization and setting equipment8.Disinfection, disinsectization and prophylaxis

	A	B	C
	Categories of vessels
—Manual resuscitation appliance	×	×
—Appliance for the administration of oxygen with pressure-reducing valve such that ship's industrial oxygen can be used, or oxygen container	×	×
—Mechanical aspirator to clear upper respiratory passages	×	×
—Cannula for mouth-to-mouth resuscitation	×	×	×
—Disposable suture stapler or suture kit with needles	×	×
—Adhesive elastic bandage	×	×	×
—Gauze strips	×
—Tubular gauze for finger bandages	×
—Sterile gauze compresses	×	×	×
—Cotton wool	×	×
—Sterile sheet for burns victims	×	×
—Triangular sling	×	×
—Disposable polyethylene gloves	×	×	×
—Adhesive dressings	×	×	×
—Sterile compression bandages	×	×	×
—Adhesive sutures or zinc oxide bandages	×	×	×
—Non-absorbable sutures with needles	×
—Vaseline gauze	×	×
—Disposable scalpels	×
—Stainless-steel instrument box	×	×
—Scissors	×	×
—Dissecting forceps	×	×
—Haemostatic clamps	×	×
—Needle forceps	×
—Disposable razors	×
—Disposable tongue depressors	×	×
—Reactive strips for urine analysis	×
—Temperature charts	×
—Medical evacuation sheets	×	×
—Stethoscope	×	×
—Aneroid sphygmomanometer	×	×
—Standard medical thermometer	×	×
—Hypothermic thermometer	×	×
—Bladder drainage instruments	×
—Rectal drip set	×
—Disposable filter infusor	×
—Urine drainage bag	×
—Disposable syringes and needles	×	×
—Catheter	×
—Bedpan	×
—Hot-water bottle	×
—Urine bottle	×
—Ice bag	×
—Malleable finger splint	×	×
—Malleable forearm and hand splint	×	×
—Inflatable splint	×	×
—Thigh splint	×	×
—Collar for neck immobilization	×	×
—Thomas splint or dimple mattress	×
—Water-disinfection compound	×
—Liquid insecticide	×
—Powder insecticide	×

III.ANTIDOTES1.MedicinesGeneralCardio-vascularGastro-intestinal systemNervous systemRespiratory systemAnti-infectiveFor external use2.Medical equipmentNecessary for the administration of oxygen (including maintenance requisites)NoteFor the detailed implementation of Section III, Member States may refer to the IMO Medical First Aid Guide for use in accidents involving dangerous goods (MFAG) contained in the 1990 consolidated edition of the IMO International Maritime Dangerous Goods Code.Any adaptation of Section III in implementation of Article 8 may take account, inter alia, of any updating of the MFAG.ANNEX IIIDANGEROUS SUBSTANCES(Article 1 (e) and Article 3 (1))The substances listed in this Annex are to be taken into account in whatever form they are carried on board, including the form of waste or cargo residues.Explosive substances and objects,Gases: compressed, liquified or dissolved under pressure,Inflammable liquids,Inflammable solids,Substances liable to spontaneous combustion,Substances which, on contact with water, give off inflammable gases,Combustible substances,Organic peroxides,Toxic substances,Infectious substances,Radioactive substances,Corrosive substances,Various dangerous substances, i.e. any other substances which experience has shown, or may show, to be dangerous, so that the provisions of Article 3 need to be applied.NoteFor the detailed implementation of this Annex, Member States may refer to the 1990 consolidated edition of the IMO International Maritime Dangerous Goods Code.Any adaptation of this Annex in implementation of Article 8 may take account, inter alia, of any updating of the IMO International Maritime Dangerous Goods Code.ANNEX IVGENERAL FRAMEWORK FOR THE INSPECTION OF VESSELS' MEDICAL SUPPLIES(Article 2 (1) (c), Article 3 (3))SECTION A.CATEGORY A VESSELSI.Details of the vesselName: …Flag: …Home port: …II.Medical supplies

1.MEDICINE1.1.Cardiovascular1.2.Gastro-intestinal system1.3.Analgesics and anti-spasmodics1.4.Nervous system1.5.Anti-allergics and anti-anaphylactics1.6.Respiratory system1.7.Anti-infection1.9.Medicines for external use(a)Skin medicines(b)Eye medicines(c)Ear medicines(d)Medicines for oral and throat infections(e)Local anaesthetics2.MEDICAL EQUIPMENT2.1.Resuscitation equipment2.2.Dressing and suturing equipment2.3.Instruments2.4.Examination and monitoring equipment2.5.Equipment for injection, perfusion, puncture and catheterization2.6.General medical equipment2.7.Immobilization and setting equipment2.8.Disinfection, disinsectization and prophylaxis3.ANTIDOTES

	Quantities required	Quantities actually carried on board	Remarks(in particular, any expiry date)
(a)Cardio-circulatory analeptics — Sympathomimetics	0	0	0
(b)Anti-angina preparations	0	0	0
(c)Diuretics	0	0	0
(d)Anti-haemorrhagics including uterotonics if there are women on board	0	0	0
(e)Anti-hypertensive	0	0	0
(a)Medicines for gastric and duodenal disorders
—Histamine H2 receptor anti-ulcer antagonists	0	0	0
—Anti-acid mucous dressings	0	0	0
(b)Anti-emetics	0	0	0
(c)Lubricant laxatives	0	0	0
(d)Anti-diarrhoeals	0	0	0
(e)Intestinal antiseptics	0	0	0
(f)Haemorrhoid preparations	0	0	0
(a)Analgesics, anti-pyretics and anti-inflammatory preparations	0	0	0
(b)Powerful analgesics	0	0	0
(c)Spasmolytics	0	0	0
(a)Anxiolytics	0	0	0
(b)Neuroleptics	0	0	0
(c)Seasickness remedies	0	0	0
(d)Anti-epileptics	0	0	0
(a)H1 Anti-histaminics	0	0	0
(b)Injectable glucocorticoids	0	0	0
(a)Bronchiospasm preparations	0	0	0
(b)Anti-tussives	0	0	0
(c)Medicines used for colds and sinusitis	0	0	0
(a)Antibiotics (at least two families)	0	0	0
(b)Anti-bacterial sulphamide	0	0	0
(c)Urinary antiseptics	0	0	0
(d)Anti-parasitics	0	0	0
(e)Intestinal anti-infectives	0	0	0
(f)Anti-tetanus vaccines and immunoglobulins	0	0	0
1.8.Compounds promoting rehydration, caloric intake and plasma expansion	0	0	0
—Antiseptic solutions	0	0	0
—Antibiotic ointments	0	0	0
—Anti-inflammatory and analgesic ointments	0	0	0
—Anti-mycotic skin creams	0	0	0
—Burn preparations	0	0	0
—Antibiotic drops	0	0	0
—Antibiotic and anti-inflammatory drops	0	0	0
—Anaesthetic drops	0	0	0
—Hypotonic myotic drops	0	0	0
—Antibiotic solutions	0	0	0
—Anaesthetic and anti-inflammatory solutions	0	0	0
—Antibiotic or antiseptic mouthwashes	0	0	0
—Local anaesthetics using freezing	0	0	0
—Local anaesthetics given by subcutaneous injection	0	0	0
—Dental anaesthetic and antiseptic mixtures	0	0	0
—Manual resuscitation appliance	0	0	0
—Appliance for the administration of oxygen with pressure-reducing valve such that ship's industrial oxygen can be used, or oxygen container	0	0	0
—Mechanical aspirator to clear upper respiratory passages	0	0	0
—Cannula for mouth-to-mouth resuscitation	0	0	0
—Disposable suture stapler or suture kit with needles	0	0	0
—Adhesive elastic bandage	0	0	0
—Gauze strips	0	0	0
—Tubular gauze for finger bandages	0	0	0
—Sterile gauze compresses	0	0	0
—Cotton wool	0	0	0
—Sterile sheet for burns victims	0	0	0
—Triangular sling	0	0	0
—Disposable polyethylene gloves	0	0	0
—Adhesive dressings	0	0	0
—Sterile compression bandages	0	0	0
—Adhesive sutures or zinc oxide bandages	0	0	0
—Non-absorbable sutures with needles	0	0	0
—Vaseline gauze	0	0	0
—Disposable scalpels	0	0	0
—Stainless-steel instrument box	0	0	0
—Scissors	0	0	0
—Dissecting forceps	0	0	0
—Haemostatic clamps	0	0	0
—Needle forceps	0	0	0
—Disposable razors	0	0	0
—Disposable tongue depressors	0	0	0
—Reactive strips for urine analysis	0	0	0
—Temperature charts	0	0	0
—Medical evacuation sheets	0	0	0
—Stethoscope	0	0	0
—Aneroid sphygmomanometer	0	0	0
—Standard medical thermometer	0	0	0
—Hypothermic thermometer	0	0	0
—Bladder drainage instruments	0	0	0
—Rectal drip set	0	0	0
—Disposable filter infusor	0	0	0
—Urine drainage bag	0	0	0
—Disposable syringes and needles	0	0	0
—Catheter	0	0	0
—Bedpan	0	0	0
—Hot-water bottle	0	0	0
—Urine bottle	0	0	0
—Ice bag	0	0	0
—Malleable finger splint	0	0	0
—Malleable forearm and hand splint	0	0	0
—Inflatable splint	0	0	0
—Thigh splint	0	0	0
—Collar for neck immobilization	0	0	0
—Thomas splint or dimple mattress	0	0	0
—Water-disinfection compound	0	0	0
—Liquid insecticide	0	0	0
—Powder insecticide	0	0	0
3.1.General	0	0	0
3.2.Cardio-vascular	0	0	0
3.3.Gastro-intestinal system	0	0	0
3.4.Nervous system	0	0	0
3.5.Respiratory system	0	0	0
3.6.Anti-infective	0	0	0
3.7.For external use	0	0	0
3.8.Other	0	0	0
3.9.Necessary for the administration of oxygen	0	0	0

Venue and date: …Captain's signature: …Approval of the competent person or authority: …SECTION B.CATEGORY B VESSELSI.Details of the vesselName: …Flag: …Home port: …II.Medical supplies

1.MEDICINE1.1.Cardiovascular1.2.Gastro-intestinal system1.3.Analgesics and anti-spasmodics1.4.Nervous system1.6.Respiratory system1.7.Anti-infection1.9.Medicines for external use(a)Skin medicines(b)Eye medicines(c)Ear medicines(d)Medicines for oral and throat infections(e)Local anaesthetics2.MEDICAL EQUIPMENT2.1.Resuscitation equipment2.2.Dressing and suturing equipment2.3.Instruments2.4.Examination and monitoring equipment2.5.Equipment for injection, perfusion, puncture and catheterization2.6.Immobilization and setting equipment3.ANTIDOTES

	Quantities required	Quantities actually carried on board	Remarks(in particular, any expiry date)
(a)Cardio-circulatory analeptics — Sympathomimetics	0	0	0
(b)Anti-angina preparations	0	0	0
(c)Diuretics	0	0	0
(d)Anti-haemorrhagics including uterotonics if there are women on board	0	0	0
(a)Medicines for gastric and duodenal disorders
—Anti-acid mucous dressings	0	0	0
(b)Anti-emetics	0	0	0
(c)Anti-diarrhoeals	0	0	0
(d)Intestinal antiseptics	0	0	0
(e)Haemorrhoid preparations	0	0	0
(a)Analgesics, anti-pyretics and anti-inflammatory preparations	0	0	0
(b)Powerful analgesics	0	0	0
(c)Spasmolytics	0	0	0
(a)Anxiolytics	0	0	0
(b)Neuroleptics	0	0	0
(c)Seasickness remedies	0	0	0
(a)Bronchiospasm preparations	0	0	0
(b)Anti-tussives	0	0	0
(c)Medicines used for colds and sinusitis	0	0	0
(a)Antibiotics (at least two families)	0	0	0
(b)Anti-bacterial sulphamide	0	0	0
(c)Anti-parasitics	0	0	0
(d)Intestinal anti-infectives	0	0	0
(e)Anti-tetanus vaccines and immunoglobulins	0	0	0
1.8.Compounds promoting rehydration, caloric intake and plasma expansion	0	0	0
—Antiseptic solutions	0	0	0
—Antibiotic ointments	0	0	0
—Anti-inflammatory and analgesic ointments	0	0	0
—Burn preparations	0	0	0
—Antibiotic drops	0	0	0
—Antibiotic and anti-inflammatory drops	0	0	0
—Anaesthetic drops	0	0	0
—Hypotonic myotic drops	0	0	0
—Antibiotic solutions	0	0	0
—Anaesthetic and anti-inflammatory solutions	0	0	0
—Antibiotic or antiseptic mouthwashes	0	0	0
—Local anaesthetics given by subcutaneous injection	0	0	0
—Dental anaesthetic and antiseptic mixtures	0	0	0
—Manual resuscitation appliance	0	0	0
—Appliance for the administration of oxygen with pressure-reducing valve such that ship's industrial oxygen can be used, or oxygen container	0	0	0
—Mechanical aspirator to clear upper respiratory passages	0	0	0
—Cannula for mouth-to-mouth resuscitation	0	0	0
—Disposable suture stapler or suture kit with needles	0	0	0
—Adhesive elastic bandage	0	0	0
—Sterile gauze compresses	0	0	0
—Cotton wool	0	0	0
—Sterile sheet for burns victims	0	0	0
—Triangular sling	0	0	0
—Disposable polyethylene gloves	0	0	0
—Adhesive dressings	0	0	0
—Sterile compression bandages	0	0	0
—Adhesive sutures or zinc oxide bandages	0	0	0
—Vaseline gauze	0	0	0
—Stainless-steel instrument box	0	0	0
—Scissors	0	0	0
—Dissecting forceps	0	0	0
—Haemostatic clamps	0	0	0
—Disposable tongue depressors	0	0	0
—Medical evacuation sheets	0	0	0
—Stethoscope	0	0	0
—Aneroid sphygmomanometer	0	0	0
—Standard medical thermometer	0	0	0
—Hypothermic thermometer	0	0	0
—Disposable syringes and needles	0	0	0
—Malleable finger splint	0	0	0
—Malleable forearm and hand splint	0	0	0
—Inflatable splint	0	0	0
—Thigh splint	0	0	0
—Collar for neck immobilization	0	0	0
3.1.General	0	0	0
3.2.Cardio-vascular	0	0	0
3.3.Gastro-intestinal system	0	0	0
3.4.Nervous system	0	0	0
3.5.Respiratory system	0	0	0
3.6.Anti-infective	0	0	0
3.7.For external use	0	0	0
3.8.Other	0	0	0
3.9.Necessary for the administration of oxygen	0	0	0

Venue and date: …Captain's signature: …Authorization by competent person or authority: …SECTION C.CATEGORY C VESSELSI.Details of the vesselName: …Flag: …Home port: …II.Medical supplies

1.MEDICINE1.1.Cardiovascular1.2.Gastro-intestinal system1.3.Analgesics and anti-spasmodics1.4.Nervous system1.5.Medicines for external use2.MEDICAL EQUIPMENT2.1.Resuscitation equipment2.2.Dressing and suturing equipment3.ANTIDOTES

	Quantities required	Quantities actually carried on board	Remarks(in particular, any expiry date)
(a)Anti-angina preparations	0	0	0
(b)Anti-haemorrhagics including uterotonics if there are women on board	0	0	0
(a)anti-emetics	0	0	0
(b)anti-diarrhoeals	0	0	0
—Analgesics, anti-pyretics and anti-inflammatory preparations	0	0	0
—Seasickness remedies	0	0	0
—Skin medicines
—Antiseptic solutions	0	0	0
—Burn preparations	0	0	0
—Cannula for mouth-to-mouth resuscitation	0	0	0
—Adhesive elastic bandage	0	0	0
—Sterile gauze compresses	0	0	0
—Disposable polyethylene gloves	0	0	0
—Adhesive dressings	0	0	0
—Sterile compression bandages	0	0	0
—Adhesive sutures or zinc oxide bandages	0	0	0
3.1.General	0	0	0
3.2.Cardio-vascular	0	0	0
3.3.Gastro-intestinal system	0	0	0
3.4.Nervous system	0	0	0
3.5.Respiratory system	0	0	0
3.6.Anti-infective	0	0	0
3.7.For external use	0	0	0
3.8.Other	0	0	0
3.9.Necessary for the administration of oxygen	0	0	0

Venue and date: …Captain's signature: …Authorization of the competent person or authority: …ANNEX VMEDICAL TRAINING OF THE CAPTAIN AND DESIGNATED WORKERS(Article 5 (3))I.1.Basic understanding of physiology, symptomatology and therapeutics.2.Elements of preventive medicine, notably individual and collective hygiene, and elements of possible prophylactic measures.3.Ability to perform basic types of treatment and supervise emergency disembarkation at sea.Person responsible for treatment aboard category A vessels should if possible receive their practical training in hospitals.4.Detailed knowledge of how to use the various remote medical consultation facilities.II.This training should take account of the programmes of instruction detailed in relevant recent international documents.

November 20, 2019	annex II	Replacement
November 20, 2019	annex IV	Replacement

Council Directive 92/29/EEC of 31 March 1992 on the minimum safety and health requirements for improved medical treatment on board vessels

Modified by

Commission Directive (EU) 2019/1834 of 24 October 2019 amending Annexes II and IV to Council Directive 92/29/EEC as regards purely technical adaptations