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VIADOLFIX Pharma 3

EUDAMED

Class I (EU MDR)

Ref 70010403Model 70030201

by Prim, S.a.

Identity

Trade Name
VIADOLFIX Pharma 3 EUDAMED
Device Name
VIADOLFIX EUDAMED
Model / Reference
70030201 EUDAMED
70010403 EUDAMED

Identifiers

Primary DI / UDI-DI
08470003285346 EUDAMED
Basic UDI-DI
843404825MALLATUBULAR59 EUDAMED
EMDN Code
M03030103 TUBULAR NET BANDAGES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

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

VIADOLFIX Pharma 3 by Prim S.a. — 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
Prim, S.a.
EUDAMED SRN
ES-MF-000004651

Sources (1)

  • EUDAMED 0a6c8f1e-adec-4291-8c1d-d7175e968a26 61 fields · synced Jun 18, 2026