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KEISEI Super Micro Forceps 13cm Titanium

EUDAMED

Class I (EU MDR)

Ref DMF-13T

by Keisei Medical Industrial Co., Ltd.

Identity

Trade Name
KEISEI Super Micro Forceps 13cm Titanium EUDAMED
Device Name
KEISEI Super Micro Forceps 13cm Titanium EUDAMED
Model / Reference
DMF-13T EUDAMED

Identifiers

Primary DI / UDI-DI
34946279748410 EUDAMED
Basic UDI-DI
B-34946279748410 EUDAMED
EMDN Code
L03130499 GRASPING FORCEPS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

KEISEI Super Micro Forceps 13cm Titanium by Keisei Medical Industrial Co., Ltd. — Class I — 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 4ddb88c0-15d0-465d-990b-e516bc7eb48f 61 fields · synced Jun 18, 2026