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Dr. Brace

by Dr. Brace LLC EUDAMED

Active European Union

Ref ID-Z3QG-K8H5-EUModel Dr. Brace OKB

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number506101344OKB123QV Basic UDI-DIDate29 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
DR. BRACE ELITE Knee Brace with Side Stabilizers & Patella Gel Pads
Model / Reference
Dr. Brace OKB, ID-Z3QG-K8H5-EU
Primary DI / UDI-DI
05061013441780
Basic UDI-DI
506101344OKB123QV
EMDN Code
M030501 Immobilisation bandages for shoulder, arm and collarbone
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000053232
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Dr. Brace LLC

See all devices from Dr. Brace LLC →

Properties

Other properties (13)

  • Sterile: No
  • 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