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SCANLAN® Finesse Micro Forceps

EUDAMED

Class I (EU MDR)

Ref 2922-00

by Scanlan International Inc.

Identity

Device Name
SCANLAN® Finesse Micro Forceps EUDAMED
Model / Reference
2922-00 EUDAMED

Identifiers

Primary DI / UDI-DI
00846159037142 EUDAMED
Basic UDI-DI
B-00846159037142 EUDAMED
EMDN Code
L031306 HEMOSTATIC FORCEPS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

SCANLAN® Finesse Micro Forceps by Scanlan International Inc — 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
US-MF-000010251
Authorised Representative
MedEnvoy Global BV NL-AR-000024028

Sources (1)

  • EUDAMED a66cf424-cd18-456e-b7c9-685f66027961 61 fields · synced Jul 8, 2026