Single-Use Patient Part (SUPP)

EUDAMED

Class IIa (EU MDR)

Ref 5201-61

by Vimex Sp. z o.o.

Identity

Device Name: Single-Use Patient Part (SUPP) EUDAMED
Model / Reference: 5201-61 EUDAMED

Identifiers

Primary DI / UDI-DI: 05907595122474 EUDAMED
Basic UDI-DI: 5907595122PV-5201SUPPAP EUDAMED
EMDN Code: A030499 ADMINISTRATION KITS - OTHER EUDAMED

Classification

Device Class: Class IIa EUDAMED
Market of Registration: Poland EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

EUDAMED

Reusable

EUDAMED

Contains Latex

EUDAMED

Reprocessed

EUDAMED

CMR Substance

EUDAMED

Human-derived

EUDAMED

Human Tissues

EUDAMED

Animal Tissues

EUDAMED

Endocrine Disruptor

EUDAMED

Administering Medicine

EUDAMED

Measuring Function

EUDAMED

Incorporates Medicinal Product

EUDAMED

Single-Use Patient Part (SUPP) by Vimex Sp. z o.o. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Source	Region	Type	Cert / Approval No.	Class	Status
EUDAMED	European Union	CE/MDR	5907595122PV-5201SUPPAP	Class IIa	Active

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Manufacturer

Manufacturer: Vimex Sp. z o.o.
EUDAMED SRN: PL-MF-000008668

Sources (1)

EUDAMED 8f9cf488-2256-4497-97fb-55dc300b89df 61 fields · synced Jun 20, 2026