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7g Black Mamba

by Ergoactives, LLC EUDAMED

Active European Union

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0852123006ERGOBAUMG3 Basic UDI-DIDate7 May 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  • Withdrawn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
Ergobaum
Primary DI / UDI-DI
00852123006991
Basic UDI-DI
0852123006ERGOBAUMG3
Direct Marketing DI
00852123006991
EMDN Code
Y12030601 Elbow crutches
Device Class
Class I
Market of Registration
Norway

Manufacturer details

EUDAMED SRN
US-MF-000015292
Authorised representative
MedEnvoy Global BV NL-AR-000024028

From the manufacturer

Manufacturer's product page: Ergobaum XG Black Mamba Carbon Fiber

Other devices from Ergoactives, LLC

See all devices from Ergoactives, 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