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Gimmi SR.1080.20

by Gimmi GmbH

Part of a family of 18 devices: see the family page

Ref SR.1080.20

Gimmi SR.1080.20 is a surgical drape clip (EU MDR Class I; FDA Class I; FDA product code MDM, Instrument, Manual, Surgical, General Use) made by Gimmi GmbH, registered in EUDAMED on 15 Jul 2026 (Basic UDI-DI 4049047SAD03ABA27DROD2) and listed in FDA GUDID since 22 May 2025 (UDI-DI 04049047778691), 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 Number4049047SAD03ABA27DROD2 Basic UDI-DI 04049047778691UDI-DIDate15 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04049047778691 UDI-DI Date22 May 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4049047SAD03ABA27DROD2 registered 15 Jul 2026 Active
  • FDA GUDID UDI-DI 04049047778691 listed 22 May 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04049047778691
  2. Registered EUDAMED 4049047SAD03ABA27DROD2

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  • Withdrawn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
Gimmi
Generic name
Surgical drape clip, reusable
Device name
Product for cleaning and storage
Model / Ref / Catalog
SR.1080.20
Description
SAFETY PIN LENGTH 200 MM
Primary DI / UDI-DI
04049047778691
Basic UDI-DI
4049047SAD03ABA27DROD2
Direct marketing DI
04049047778691
FDA product code
MDM
EMDN code
S9080 Devices for sterilisation (excluding cat. d - z) - accessories
GMDN term
Surgical drape clip, 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: Surgical drape clip, reusable

Similar devices in this category

Other devices filed under DEVICES FOR STERILISATION (EXCLUDING CAT. D - Z) - ACCESSORIES.

Other devices from Gimmi GmbH

See all devices from Gimmi GmbH →

Properties

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