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00502316300

by Conmed Corporation

Ref 5023-163

00502316300 (5023-163) is a device classified as Class IIa in the EU and Class I in the US made by Conmed Corporation, registered in EUDAMED on 7 Apr 2026 (Basic UDI-DI B-10845854009499) and listed in FDA GUDID since 24 Sep 2020 (UDI-DI 10845854009499), 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-10845854009499 Basic UDI-DI 10845854009499UDI-DIDate7 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854009499 UDI-DI Date24 Sep 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10845854009499 registered 7 Apr 2026 Active
  • FDA GUDID UDI-DI 10845854009499 listed 24 Sep 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10845854009499
  2. Registered EUDAMED B-10845854009499

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  • Withdrawn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
Surgical saw blade, sagittal, single-use
Device name
Orthopedic, Non-active, Handpiece Blade, Oscillating
Model / Ref / Catalog
5023-163, 00502316300
Primary DI / UDI-DI
10845854009499
Basic UDI-DI
B-10845854009499
FDA product code
GFA
EMDN code
K030203 Arthroscopy blades, single-use
GMDN term
Surgical saw blade, sagittal, single-use
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
878.4820
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Size
Width — 10 Millimeter
Height — 0.4 Millimeter
Length — 18.5 Millimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
5023-163
GUDID
00502316300
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: Surgical saw blade, sagittal, single-use

Similar devices in this category

Other devices filed under ARTHROSCOPY BLADES, SINGLE-USE.

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)