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Powerflex Afd

by Andover Healthcare Inc. United States EUDAMED

Ref 3722WH-016Model POWERFLEX AFD

EMDN M030402020101

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0724004PowerFlexAFD7V Basic UDI-DIDate18 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Coflex
Model / Reference
POWERFLEX AFD, 3722WH-016
Primary DI / UDI-DI
00724004607613
Basic UDI-DI
0724004PowerFlexAFD7V
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 & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED 00724004607613|0724004POWERFLEXAFD7V 61 fields · synced 24 Oct 2026