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devemed 1065

by devemed GmbH

Ref 1065

devemed 1065 is a Class I device made by devemed GmbH, registered in EUDAMED on 15 Jul 2026 (Basic UDI-DI 4061644PG0205032M) and listed in FDA GUDID since 8 Apr 2020 (UDI-DI 04061644001552), active as of 23 Oct 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4061644PG0205032M Basic UDI-DI 04061644001552UDI-DIDate15 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04061644001552 UDI-DI Date8 Apr 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4061644PG0205032M registered 15 Jul 2026 Active
  • FDA GUDID UDI-DI 04061644001552 listed 8 Apr 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04061644001552
  2. Registered EUDAMED 4061644PG0205032M

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  • Withdrawn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
devemed
Generic name
Towel clamp, reusable
Device name
Towel Clips
Model / reference
1065
Description
Towel clip "Backhaus" | 110 mm
Primary DI / UDI-DI
04061644001552
Basic UDI-DI
4061644PG0205032M
Direct marketing DI
04061644001552
FDA product code
HTD
EMDN code
L031305 Forceps for fabrics and bandages, reusable
GMDN term
Towel clamp, 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

Similar devices in this category

Other devices filed under GENERAL SURGERY FORCEPS, REUSABLE.

Other devices from devemed GmbH

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (21, all answered No)