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G-Mesh

EUDAMED

Class IIb (EU MDR)

Ref MA-271-GMP2-001Model Posterior 2

by Tricomed S.a.

Identity

Trade Name
G-Mesh EUDAMED
Device Name
G-Mesh EUDAMED
Model / Reference
Posterior 2 EUDAMED
MA-271-GMP2-001 EUDAMED

Identifiers

Primary DI / UDI-DI
05900516862572 EUDAMED
Basic UDI-DI
B-05900516862572 EUDAMED
EMDN Code
P080499 FEMALE GENITAL SYSTEM PROSTHESES - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Poland EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

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

G-Mesh by Tricomed S.a. — Class IIb — 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

Manufacturer
Tricomed S.a.
EUDAMED SRN
PL-MF-000002483

Sources (1)

  • EUDAMED d96bb383-5f9e-456a-a746-05c2952ad242 61 fields · synced Jun 19, 2026