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Neoveil

EUDAMED

Class III (EU MDR)

Ref NV-ET-M45E-2

by Gunze Limited

Identity

Trade Name
NEOVEIL EUDAMED
Device Name
NEOVEIL EUDAMED
Model / Reference
NV-ET-M45E-2 EUDAMED

Identifiers

Primary DI / UDI-DI
04547301462541 EUDAMED
Basic UDI-DI
B-04547301462541 EUDAMED
EMDN Code
P900201 POLYGLYCOLIC ACID AND ASSOCIATIONS MESHES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Spain 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

Neoveil by Gunze Limited — Class III — 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
Gunze Limited
EUDAMED SRN
JP-MF-000015551
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED bcae333a-09cf-4b87-978e-f66df4a04c93 61 fields · synced May 23, 2026