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Argo Knotless K475RTAP

by Conmed Corporation

Ref K475RTAP

Argo Knotless K475RTAP is a Class I device made by Conmed Corporation, registered in EUDAMED on 27 May 2026 (Basic UDI-DI B-30653405988360) and listed in FDA GUDID since 13 Jan 2023 (UDI-DI 30653405988360), 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-30653405988360 Basic UDI-DI 30653405988360UDI-DIDate27 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number30653405988360 UDI-DI Date13 Jan 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-30653405988360 registered 27 May 2026 Active
  • FDA GUDID UDI-DI 30653405988360 listed 13 Jan 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 30653405988360
  2. Registered EUDAMED B-30653405988360

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  • Withdrawn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
Argo Knotless
Generic name
Bone tap, reusable
Device name
Reusable Manual Surgical Instruments
Model / Ref / Catalog
K475RTAP
Primary DI / UDI-DI
30653405988360
Basic UDI-DI
B-30653405988360
FDA product code
HWX
EMDN code
L090999 Orthopaedic surgery cutting instruments, reusable - other
GMDN term
Bone tap, reusable
Device class
Class I
Regulation number
888.4540
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

Similar devices in this category

Other devices filed under ORTHOPAEDIC SURGERY CUTTING INSTRUMENTS, REUSABLE - OTHER.

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)