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Silver Foam Medium

EUDAMED

Class III (EU MDR)

Ref XF-AGMFOAM2

by Genadyne Biotechnologies, Inc.

Identity

Trade Name
Silver Foam Medium EUDAMED
Device Name
Silver Foam Medium EUDAMED
Model / Reference
XF-AGMFOAM2 EUDAMED

Identifiers

Primary DI / UDI-DI
00849405000464 EUDAMED
Basic UDI-DI
B-00849405000464 EUDAMED
EMDN Code
M04040801 SILVER DRESSINGS, NON-COMBINED EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Silver Foam Medium by Genadyne Biotechnologies Inc. — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
US-MF-000017992
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 5ad3a059-c67a-4ce3-9296-a61fb6444d8f 61 fields · synced Jul 31, 2026