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Aggressor

by Conmed Corporation 3 variants

Ref 31.10034, 31.16235

Aggressor (31.10034) is a Class I device made by Conmed Corporation, registered in EUDAMED on 29 Apr 2026 (Basic UDI-DI B-10845854024539) and listed in FDA GUDID since 24 Sep 2020 (UDI-DI 10845854024539), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10845854024539 Basic UDI-DI Date29 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854024539 UDI-DI Date24 Sep 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10845854024539 registered 29 Apr 2026 Active
  • FDA GUDID UDI-DI 10845854024539 listed 24 Sep 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10845854024539
  2. Registered EUDAMED B-10845854024539

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  • Withdrawn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

Generic name
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Device name
Orthopedic, Non-active, Reusable Surgical Instrument, Cutting
Model / Ref / Catalog
31.10034, 31.16235
Primary DI / UDI-DI
10845854024539, 10845854024553
Basic UDI-DI
B-10845854024539, B-10845854024553
FDA product code
GEN
EMDN code
L03130401 Tissue and organ grasping forceps, reusable
GMDN term
Surgical soft-tissue manipulation forceps, scissors-like, reusable
Device class
Class I
Regulation number
878.4800
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 130 Millimeter
Width — 3.4 Millimeter
Angle — 15 degree

Manufacturer details

EUDAMED SRN
US-MF-000012663
Authorised representative
MDSS GmbH DE-AR-000005430

Related devices

Category: Ophthalmic soft-tissue manipulation forceps, tweezers-like, reusable

Similar devices in this category

Other devices filed under TISSUE AND ORGAN GRASPING FORCEPS, REUSABLE.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

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