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Aesculap OM761R

by Aesculap AG

Ref OM761R

Aesculap OM761R is a Class I device made by Aesculap AG, registered in EUDAMED on 16 Sep 2025 (Basic UDI-DI 4039239000001301ZL) and listed in FDA GUDID since 23 Apr 2020 (UDI-DI 04038653180189), 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 Number4039239000001301ZL Basic UDI-DI 04038653180189UDI-DIDate16 Sep 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04038653180189 UDI-DI Date23 Apr 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4039239000001301ZL registered 16 Sep 2025 Active
  • FDA GUDID UDI-DI 04038653180189 listed 23 Apr 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04038653180189
  2. Registered EUDAMED 4039239000001301ZL

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  • Withdrawn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
Nasal snare, reusable
Device name
Tonsil snare
Model / Ref / Catalog
OM761R
Primary DI / UDI-DI
04038653180189
Basic UDI-DI
4039239000001301ZL
Direct marketing DI
04038653180189
FDA product code
KBZ
EMDN code
L149008 ENT enucleation instruments, reusable
GMDN term
Nasal snare, reusable
Device class
Class I
Regulation number
874.4420
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: Nasal snare, reusable

Similar devices in this category

Other devices filed under ENT INSTRUMENTS, REUSABLE - VARIOUS.

Other devices from Aesculap AG

See all devices from Aesculap AG →

Properties

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