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Aesculap PL817R

by Aesculap AG

Ref PL817R

Aesculap PL817R is a Class I device made by Aesculap AG, registered in EUDAMED on 11 Aug 2026 (Basic UDI-DI 40392390000019122S) and listed in FDA GUDID since 24 Apr 2020 (UDI-DI 04046963848064), active as of 12 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number40392390000019122S Basic UDI-DI 04046963848064UDI-DIDate11 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04046963848064 UDI-DI Date24 Apr 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 40392390000019122S registered 11 Aug 2026 Active
  • FDA GUDID UDI-DI 04046963848064 listed 24 Apr 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04046963848064
  2. Registered EUDAMED 40392390000019122S

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Aesculap
Generic name
Skin staple remover, reusable
Device name
DS-SINGLE FIRE lap. removal forc. M
Model / Ref / Catalog
PL817R
Primary DI / UDI-DI
04046963848064
Basic UDI-DI
40392390000019122S
Direct marketing DI
04046963848064
FDA product code
GDO
EMDN code
H020303 Clip appliers
GMDN term
Skin staple remover, reusable
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Skin staple remover, reusable

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Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)