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Artiflex®

EUDAMED

Class I (EU MDR)

Ref 09046-00

by BSN Medical Inc.

Identity

Trade Name
Artiflex® EUDAMED
Device Name
ARTIFLEX EUDAMED
Model / Reference
09046-00 EUDAMED

Identifiers

Primary DI / UDI-DI
04042809075069 EUDAMED
Basic UDI-DI
4042809400422368F EUDAMED
Unit of Use DI
04042809467123 EUDAMED
EMDN Code
M03050202 SYNTHETIC CAST BANDAGES AND SPLINTS 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: Cotton wool roll, sterile

Artiflex® by Bsn Medical, Inc. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Cotton wool roll, sterile.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
BSN Medical Inc.
EUDAMED SRN
US-MF-000019174
Authorised Representative
BSN medical GmbH DE-AR-000005791

Sources (1)

  • EUDAMED 23bb0542-7861-49cc-8050-d7694f49833e 61 fields · synced Sep 18, 2026