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Conmed AP1520-061

by Conmed Corporation

Ref AP1520-061

Conmed AP1520-061 is an orthopaedic bur (EU MDD Class I; FDA Class I; FDA product code GFG, Bit, Surgical) made by Conmed Corporation, registered in EUDAMED on 26 May 2026 (Basic UDI-DI B-10845854030318) and listed in FDA GUDID since 28 Apr 2020 (UDI-DI 10845854030318), 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-10845854030318 Basic UDI-DI 10845854030318UDI-DIDate26 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854030318 UDI-DI Date28 Apr 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-10845854030318 registered 26 May 2026 Active
  • FDA GUDID UDI-DI 10845854030318 listed 28 Apr 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10845854030318
  2. Registered EUDAMED B-10845854030318

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  • Withdrawn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
Orthopaedic bur, reusable
Device name
Reusable Manual Surgical Instruments
Model / Ref / Catalog
AP1520-061
Primary DI / UDI-DI
10845854030318
Basic UDI-DI
B-10845854030318
FDA product code
GFG
EMDN code
L0922 Orthopaedic surgery guides, reusable
GMDN term
Orthopaedic bur, reusable
Device class
Class I
Regulation number
878.4820
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
Outer Diameter — 1.5 Millimeter

Related devices

Category: Orthopaedic bur, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC SURGERY GUIDES, REUSABLE.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

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