← Back to catalogue

Relifoam Silicone Hydrophilic Foam Dressing

EUDAMED

Class I (EU MDR)

Ref 4138-004-(7.5cm x 7.5cm)Model HYFD

by Dynamic Techno Medicals Pvt Ltd

Identity

Trade Name
Relifoam Silicone Hydrophilic Foam Dressing EUDAMED
Device Name
Hydrophilic Foam Dressings EUDAMED
Model / Reference
HYFD EUDAMED
4138-004-(7.5cm x 7.5cm) EUDAMED

Identifiers

Primary DI / UDI-DI
08904044234082 EUDAMED
Basic UDI-DI
89040442HFWDQP EUDAMED
EMDN Code
M04040601 POLYURETHANE DRESSINGS, NON-COMBINED EUDAMED

Classification

Device Class
Class I EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Relifoam Silicone Hydrophilic Foam Dressing by Dynamic Techno Medicals Pvt Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Negative-pressure wound therapy system foam dressing, non-antimicrobial.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 587a5684-87b6-43f8-ad49-1991e86fb39d 61 fields · synced Jun 20, 2026