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Coflex Med

by Andover Healthcare Inc. EUDAMED

Active European Union

Ref 7100CP-030Model CoFlex Med

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0724004CoFlexMED9A Basic UDI-DIDate25 Mar 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  • Withdrawn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
CoFlex Med, 7100CP-030
Primary DI / UDI-DI
00724004400900
Basic UDI-DI
0724004CoFlexMED9A
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

From the manufacturer

Manufacturer's product page: CoFlex® Med

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