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Optomesh SUPERULTRALIGHT

EUDAMED

Class IIb (EU MDR)

Ref MB-271-OPSL-002Model 50x100 mm

by Tricomed S.a.

Identity

Trade Name
Optomesh SUPERULTRALIGHT EUDAMED
Device Name
Optomesh SUPERULTRALIGHT EUDAMED
Model / Reference
50x100 mm EUDAMED
MB-271-OPSL-002 EUDAMED

Identifiers

Primary DI / UDI-DI
05906146501034 EUDAMED
Basic UDI-DI
B-05906146501034 EUDAMED
EMDN Code
P900202 POLYPROPYLENE SURGICAL MESHES 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

Optomesh SUPERULTRALIGHT 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 7133a3f2-d157-4146-82b6-02c239765137 61 fields · synced Jul 25, 2026