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Argo Knotless K4755RBP

by Conmed Corporation

Ref K4755RBP

Argo Knotless K4755RBP is a Class I device made by Conmed Corporation, registered in EUDAMED on 31 Jan 2026 (Basic UDI-DI 084585464942F7) and listed in FDA GUDID since 25 Sep 2021 (UDI-DI 30845854083233), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

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/MDR EUDAMED Number084585464942F7 Basic UDI-DI 30845854083233UDI-DIDate31 Jan 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number30845854083233 UDI-DI Date25 Sep 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 084585464942F7 registered 31 Jan 2026 Active
  • FDA GUDID UDI-DI 30845854083233 listed 25 Sep 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 30845854083233
  2. Registered EUDAMED 084585464942F7

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Argo Knotless
Generic name
Orthopaedic broach
Device name
Orthopedic, Non-active, Reusable Surgical Instrument, Cutting
Model / Ref / Catalog
K4755RBP
Primary DI / UDI-DI
30845854083233
Basic UDI-DI
084585464942F7
Direct marketing DI
10845854083239
FDA product code
HWX
EMDN code
L0999 Orthopaedic and traumatological surgery instruments, reusable - other
GMDN term
Orthopaedic broach
Device class
Class I
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Sterilise before useEUDAMED
Yes
GUDID
No

Registry differences

EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:

  • Sterilise before use UDI-DI 30845854083233: EUDAMED states Yes, FDA GUDID states No.

Similar devices in this category

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

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

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