Skip to content

Powerflex 6YD

by Andover Healthcare Inc. EUDAMED

Active European Union

Ref 3740WH-012Model POWERFLEX 6YD

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0724004PowerFlex6YD84 Basic UDI-DIDate15 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Coflex
Model / Reference
POWERFLEX 6YD, 3740WH-012
Primary DI / UDI-DI
10724004402444
Basic UDI-DI
0724004PowerFlex6YD84
EMDN Code
M030402020101 Elastic support bandages, cohesive, extensible in one direction, high extensibility
Device Class
Class I
Market of Registration
Denmark

Manufacturer details

EUDAMED SRN
US-MF-000035055
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Andover Healthcare Inc.

See all devices from Andover Healthcare Inc. →

Properties

  • Contains Latex

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Reusable: 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