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Conmed 9893

by Conmed Corporation

Ref 9893

Conmed 9893 is a device classified as Class IIa in the EU and Class I in the US made by Conmed Corporation, registered in EUDAMED on 9 Apr 2026 (Basic UDI-DI B-10845854018965) and listed in FDA GUDID since 11 Oct 2021 (UDI-DI 10845854018965), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10845854018965 Basic UDI-DI 10845854018965UDI-DIDate9 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854018965 UDI-DI Date11 Oct 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10845854018965 registered 9 Apr 2026 Active
  • FDA GUDID UDI-DI 10845854018965 listed 11 Oct 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10845854018965
  2. Registered EUDAMED B-10845854018965

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  • Withdrawn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
Conmed
Generic name
Suturing unit, single-use
Device name
Orthopedic, Non-active, Instrument, Suture Retriever
Model / Ref / Catalog
9893
Primary DI / UDI-DI
10845854018965
Basic UDI-DI
B-10845854018965
FDA product code
LXH
EMDN code
H900899 Single-use instruments for sutures - other
GMDN term
Suturing unit, single-use
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
888.4540
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class I

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Suturing unit, single-use

Similar devices in this category

Other devices filed under SINGLE-USE INSTRUMENTS FOR SUTURES - OTHER.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)