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ActiFast Green

by Lohmann & Rauscher Medical UK Ltd 4 variants

Ref 88575

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number503769688573GS Basic UDI-DI 05037696400277UDI-DIDate5 Aug 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
ActiFast Red 2 way stretch tubular retention bandage 3.5cm x 1 m
Model / Reference
88575
Primary DI / UDI-DI
05037696400277
Basic UDI-DI
503769688573GS
EMDN Code
M03030103 Tubular net bandages
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
UK-MF-000036885
Authorised representative
Lohmann & Rauscher International GmbH & Co. KG DE-AR-000005187

Other devices from Lohmann & Rauscher Medical UK Ltd

See all devices from Lohmann & Rauscher Medical UK Ltd →

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