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Relifoam Silicone Hydrophilic Foam Dressing

by Dynamic Techno Medicals Pvt Ltd 8 variants

Ref 4138-005-(12.5cm x 12.5cm)Model HYFD

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number89040442HFWDQP Basic UDI-DI 08904044213988UDI-DIDate14 Apr 2026RegisteredStatusActive EUDAMED: not on the EU market

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Hydrophilic Foam Dressings
Model / Reference
HYFD, 4138-005-(12.5cm x 12.5cm)
Primary DI / UDI-DI
08904044213988
Basic UDI-DI
89040442HFWDQP
EMDN Code
M04040601 Polyurethane dressings, non-combined
Device Class
Class I

Manufacturer details

EUDAMED SRN
IN-MF-000017845
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Related devices

Category: Negative-pressure wound therapy system foam dressing, non-antimicrobial

Properties

  • Sterile

Other properties (12)

  • 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