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Folfusor

EUDAMED

Class IIa (EU MDR)

Ref 2C4156K

by Baxter Healthcare SA

Identity

Trade Name
FOLFUSOR EUDAMED
Device Name
Infusor EUDAMED
Model / Reference
2C4156K EUDAMED

Identifiers

Primary DI / UDI-DI
00085412461007 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

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

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 60087ee1-4242-4a5e-989c-1aeaa1f9170b 61 fields · synced Jun 19, 2026