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Accolade 6720-0330

by Howmedica Osteonics Corp.

Ref 6720-0330Model 08858251004330SQ

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

CE MDR

Valid until

21 Nov 2031

CE MDR certificate

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

1 certificate

Certifier BSI Group The Netherlands B.V.

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 Number08858251004330SQ Basic UDI-DIDate28 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04546540664464 UDI-DIDate24 Sep 2015ListedStatusListed GUDID: in commercial distribution

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR 730270 Active Reissued

    Technical documentation EU MDR

    Notified body
    BSI Group The Netherlands B.V. 2797
    Issued
    9 Sep 2026
    Expires
    21 Nov 2031
    Valid from
    22 Nov 2026

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  • Withdrawn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
Accolade
Generic Name
Coated hip femur prosthesis, modular
Device Name
DD-006 - Accolade II
Model / Ref / Catalog
6720-0330, 08858251004330SQ
Primary DI / UDI-DI
04546540664464
Basic UDI-DI
08858251004330SQ
FDA Product Code
MBL, MEH, KWY, LPH, KWZ, MAY, KWL, LZO, JDI, LWJ
EMDN Code
P090804010202 Uncemented femoral stems for primary implant, with fixed neck, anatomical
GMDN Term
Coated hip femur prosthesis, modular
Device Class
Class III EUDAMED
Class II GUDID
Regulation Number
888.3358, 888.3353, 888.3390, 888.3310, 888.3360, 888.3350
Market of Registration
Netherlands
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class III
GUDID
Class II

Other devices from Howmedica Osteonics Corp.

See all devices from Howmedica Osteonics Corp. →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number

Other properties (19)

  • 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
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No