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Diamond Abrasor, Ball Tip, Coarse

by Joimax GmbH 7 variants

Ref JSBDA274544C

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

CE MDR CE MDD

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED NumberB-04250337116479 Basic UDI-DI 04250337116479UDI-DIDate22 Feb 2024RegisteredStatusActive
European UnionCE/MDD EUDAMED NumberB-04250337116479 Basic UDI-DI 04250337116479UDI-DIDate22 Feb 2024RegisteredStatusActive
United StatesGUDID listing GUDID Number04250337116479 UDI-DI Date30 Dec 2022ListedStatusListed 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  • Withdrawn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, CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Diamond Abrasor, Ball Tip, Coarse EUDAMED
Diamon Abrasor GUDID
Generic Name
Arthroscopic shaver system blade, single-use
Device Name
Barrel Cutter, Barrel Tip, with distal protection
Model / Ref / Catalog
JSBDA274544C
Primary DI / UDI-DI
04250337116479
Basic UDI-DI
B-04250337116479, 42503371DEFLRESAK
Direct Marketing DI
04250337116479
FDA Product Code
HWE
EMDN Code
Z12130585 Motorised orthopaedic surgery system instruments - consumables
GMDN Term
Arthroscopic shaver system blade, single-use
Device Class
Class IIa EUDAMED
Class I GUDID
Regulation Number
878.4820
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIa
GUDID
Class I

Manufacturer details

EUDAMED SRN
DE-MF-000009201

Related devices

Category: Spinal shaver system blade

Other devices from Joimax GmbH

See all devices from Joimax GmbH →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (17)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No