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SCANLAN® Muscle Biopsy Cannula

EUDAMED

Class I (EU MDR)

Ref 4909-96

by Scanlan International Inc.

Identity

Device Name
SCANLAN® Muscle Biopsy Cannula EUDAMED
Model / Reference
4909-96 EUDAMED

Identifiers

Primary DI / UDI-DI
00846159023183 EUDAMED
Basic UDI-DI
B-00846159023183 EUDAMED
EMDN Code
L030101 SUCTION AND IRRIGATION SURGICAL CANNULAS AND HANDPIECES, 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

Category: Surgical/emergency suction cannula, non-illuminating, reusable

SCANLAN® Muscle Biopsy Cannula by Scanlan International Inc — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/emergency suction cannula, non-illuminating, reusable.

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 da0dac86-2c12-4899-b84c-018084b6ba65 61 fields · synced Jun 19, 2026