← Back to catalogue

Fodera HMF-HYDRO

EUDAMED

Class I (EU MDR)

Ref HMF-HYDRO

by Health Medical Fab Srl

Identity

Device Name
Fodera HMF-HYDRO EUDAMED
Model / Reference
HMF-HYDRO EUDAMED

Identifiers

Primary DI / UDI-DI
08052675900354 EUDAMED
Basic UDI-DI
805267590HYDROHX EUDAMED
EMDN Code
V0880 MEDICAL SUPPORT EQUIPMENT - ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

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

Fodera HMF-HYDRO by Health Medical Fab Srl — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

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
IT-MF-000050672

Sources (1)

  • EUDAMED e32da19d-7a40-47c2-a17f-51fadac9031d 61 fields · synced Jun 18, 2026