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Optomesh SUPERULTRALIGHT

EUDAMED

Class IIb (EU MDR)

Ref MB-271-OPSL-005Model 80x80 mm

by Tricomed S.a.

Identity

Trade Name
Optomesh SUPERULTRALIGHT EUDAMED
Device Name
Optomesh SUPERULTRALIGHT EUDAMED
Model / Reference
80x80 mm EUDAMED
MB-271-OPSL-005 EUDAMED

Identifiers

Primary DI / UDI-DI
05906146501096 EUDAMED
Basic UDI-DI
B-05906146501096 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 094b3d1a-88a3-44e4-a5f9-b6ebb0c25905 61 fields · synced Jul 22, 2026