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G-plus safe pad

EUDAMED

Class I (EU MDR)

Ref '002.HC.040

by Pharmaplast

Identity

Trade Name
G-plus safe pad EUDAMED
Device Name
Vilowond® Gauze & Vilowond® Nonwoven EUDAMED
Model / Reference
'002.HC.040 EUDAMED

Identifiers

Primary DI / UDI-DI
05205962008155 EUDAMED
Basic UDI-DI
62220238VilowondGNWBP EUDAMED
EMDN Code
M0201020101,M0202010101 EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Greece 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

G-plus safe pad by Pharmaplast — 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
Pharmaplast
EUDAMED SRN
EG-MF-000004501
Authorised Representative
E C REP LIMITED IE-AR-000003995

Sources (1)

  • EUDAMED 00c45eab-292b-47f1-a467-91414fee4e96 61 fields · synced Jul 31, 2026