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SCANLAN®Ochsner Forceps

EUDAMED

Class I (EU MDR)

Ref 4160-06

by Scanlan International Inc.

Identity

Device Name
SCANLAN®Ochsner Forceps EUDAMED
Model / Reference
4160-06 EUDAMED

Identifiers

Primary DI / UDI-DI
00846159038286 EUDAMED
Basic UDI-DI
B-00846159038286 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®Ochsner 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 778bc505-5b0b-4ee1-b3c7-80bc74a24ce4 61 fields · synced Jul 27, 2026