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Tifon Hidrofil

EUDAMED

Class I (EU MDR)

Ref PRODT01

by Prodconfarm Srl

Identity

Device Name
TIFON HIDROFIL EUDAMED
Model / Reference
PRODT01 EUDAMED

Identifiers

Primary DI / UDI-DI
05944759041042 EUDAMED
Basic UDI-DI
5944759041PRODT015T EUDAMED
Direct Marketing DI
05944759041042 EUDAMED
EMDN Code
M0201020102 COTTON GAUZES, FOLDED, WITHOUT X-RAY DETECTABLE THREAD, NON-STERILE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Romania 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

Tifon Hidrofil by Prodconfarm 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

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Manufacturer

Manufacturer
Prodconfarm Srl
EUDAMED SRN
RO-MF-000017975

Sources (1)

  • EUDAMED 28a8cd65-2501-45ae-ba2b-c985a428a2e4 61 fields · synced Jun 18, 2026