Endoplast ApS

Denmark DK-MF-000001268 Last updated 21 Oct 2026

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Devices: 1
Registries: EUDAMED
FDA recalls: 0

Catalogue1

Retroplast Ref RP01

Class IIa EUDAMED Active

EUDAMED certificates1

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

Intertek Medical Notified Body AB 2862 1 certificate

28620127093-02 Supplemented

Quality assurance EU MDR

Issued
31 Aug 2026

Expires
24 Aug 2027

Reason
Other

Notified bodies

Intertek Medical Notified Body AB 2862

Information

Country: Denmark
Address: 4, Håndværkervej , Hårlev, Denmark
Website: www.endoplast.com
Email: [email protected]
Phone: +4523722599
PRRC contact: Paul Clarke
EUDAMED SRN: DK-MF-000001268