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Arthrex® AR-4020C-06D

by Arthrex, Inc.

Ref AR-4020C-06D

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

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0888867BIntScrwImpSys00ZN Basic UDI-DI 00888867483927UDI-DIDate1 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00888867483927 UDI-DI Date6 Nov 2025ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

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  • Withdrawn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
Arthrex®
Generic Name
Bioabsorbable orthopaedic bone screw
Device Name
Bioabsorbable Interference Screw Implant Systems
Model / Ref / Catalog
AR-4020C-06D
Primary DI / UDI-DI
00888867483927
Basic UDI-DI
0888867BIntScrwImpSys00ZN
FDA Product Code
MAI
EMDN Code
P09120606 Osteosynthesis devices, biodegradable screws and bars
GMDN Term
Bioabsorbable orthopaedic bone screw
Device Class
Class III EUDAMED
Class II GUDID
Regulation Number
888.3030
Medical Purpose
Procedure Packs are combinations of medical devices packaged together and placed on the market with the purpose of treatment for orthopedic pathologies
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class III
GUDID
Class II

Other devices from Arthrex, Inc.

See all devices from Arthrex, Inc. →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date

Other properties (7)

  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No