← Back to catalogue

SCANLAN® Gerald Forceps

EUDAMED

Class I (EU MDR)

Ref 3003-760N

by Scanlan International Inc.

Identity

Device Name
SCANLAN® Gerald Forceps EUDAMED
Model / Reference
3003-760N EUDAMED

Identifiers

Primary DI / UDI-DI
00846159012446 EUDAMED
Basic UDI-DI
B-00846159012446 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® Gerald 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000010251
Authorised Representative
MedEnvoy Global BV NL-AR-000024028

Sources (1)

  • EUDAMED d318d9f8-7861-452e-ae93-14cfe39227c9 61 fields · synced Sep 17, 2026