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Nylon Suture

EUDAMED

Class IIb (EU MDR)

Ref 5R23 12-0N

by Keisei Medical Industrial Co., Ltd.

Identity

Device Name
Nylon Suture EUDAMED
Model / Reference
5R23 12-0N EUDAMED

Identifiers

Primary DI / UDI-DI
34946279743644 EUDAMED
Basic UDI-DI
B-34946279743644 EUDAMED
EMDN Code
H010201010101 POLYAMIDE MONOFILAMENT WITH NEEDLE EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Italy 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

Nylon Suture by Keisei Medical Industrial Co., Ltd. — 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

EUDAMED SRN
JP-MF-000021775
Authorised Representative
mdi Europa GmbH DE-AR-000006218

Sources (1)

  • EUDAMED c7e1f624-cc5e-496e-a43f-de695d28d9c3 61 fields · synced Jun 19, 2026