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Employment Department (radiation safety) / Ministry of Health Β· Middle East & Africa

Seychelles medical device regulatory resources

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1 free resources0/25 topics with records4 regulations tracked

Everything we track for Seychelles

Structured regulatory requirements

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0 of 25 research dimensions currently covered Β· 0 official sources

Market entry

D01

Authority & regime

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D02

Legal basis & guidance

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D03

Device definition & scope

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D04

Classification rules

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D05

Registration pathways

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D06

Reliance & recognition

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D07

Economic-operator roles

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D08

Establishment, import & distribution

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D09

Dossier requirements

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D10

Official forms & portals

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Submission & evidence

D11

Label, IFU & language

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D12

QMS, audit & inspection

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D13

Standards, testing & ancillary approvals

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D14

Fees

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D15

Review clocks

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D16

Approval validity & renewal

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Lifecycle & post-market

D17

Change control

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D18

UDI, listing & traceability

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D19

Clinical investigation & performance

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D20

Special access & derogation

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D21

Manufacturer PMS

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D22

Vigilance & incident reporting

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D23

Recall, FSCA & market surveillance

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D24

Advertising, claims & promotion

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D25

Submission communications & appeal

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Official Employment Department (radiation safety) / Ministry of Health rules and guidance Β· 4 of 4 documents linked to official sources

S.I. 87 of 2023Customs Management (Prohibited and Restricted Goods) Regulations, 2023
RegistrationVerified
S.I. 113 of 2022Customs Management (Tariff and Classification of Goods) Regulations, 2022
ClassificationVerified
S.I. 88 of 2020Customs Management (Tariff and Classification of Goods) (Amendment) (No.3) Regulations, 2020
ClassificationVerified
Act 17 of 2014Radiation Safety and Security Act, 2014
GeneralVerified
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