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Folfusor

EUDAMED

Class IIa (EU MDR)

Ref M2C4063K

by Baxter Healthcare SA

Identity

Trade Name
FOLFUSOR EUDAMED
Device Name
Infusor EUDAMED
Model / Reference
M2C4063K EUDAMED

Identifiers

Primary DI / UDI-DI
00197886006490 EUDAMED
Basic UDI-DI
0085412GMN00000000002106U EUDAMED
EMDN Code
A05010101 ELASTOMERIC SYSTEMS - FIXED FLOW W/O ADDITIONAL BOLUS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

Yes

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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Elastomeric infusion pump system

Folfusor by Baxter Healthcare SA — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Elastomeric infusion pump system.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CH-MF-000026124
Authorised Representative
Baxter Deutschland GmbH DE-AR-000010308

Sources (1)

  • EUDAMED 3f9d3cf1-1b73-41e0-97ee-cbee34d59179 61 fields · synced Jul 20, 2026