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Foreign body forceps 75D866/55

by Spiggle & Theis Medizintechnik GmbH

Ref 75D866/55

Foreign body forceps 75D866/55 is a Class I device made by Spiggle & Theis Medizintechnik GmbH, registered in EUDAMED on 30 Sep 2026 (Basic UDI-DI B-04250381862209) and listed in FDA GUDID since 19 Sep 2025 (UDI-DI 04250381862209), active as of 23 Oct 2026.

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

CE MDD

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/MDD EUDAMED NumberB-04250381862209 Basic UDI-DI 04250381862209UDI-DIDate30 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04250381862209 UDI-DI Date19 Sep 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04250381862209 registered 30 Sep 2026 Active
  • FDA GUDID UDI-DI 04250381862209 listed 19 Sep 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250381862209
  2. Registered EUDAMED B-04250381862209

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Foreign body forceps
Generic name
ENT soft-tissue cutting forceps
Device name
Biopsy forceps, Foreign body forceps
Model / Ref / Catalog
75D866/55
Primary DI / UDI-DI
04250381862209
Basic UDI-DI
B-04250381862209
FDA product code
KAE
EMDN code
L03130402 Forceps for external bodies, reusable
GMDN term
ENT soft-tissue cutting forceps
Device class
Class I
Regulation number
874.4420
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: ENT soft-tissue cutting forceps

Similar devices in this category

Other devices filed under FORCEPS FOR EXTERNAL BODIES, REUSABLE.

Other devices from Spiggle & Theis Medizintechnik GmbH

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Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)