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APL2002/1 Set mit Anstechdorn

EUDAMED

Class IIa (EU MDR)

Ref 52011Model Infusionsset

by PFM medical mepro GmbH

Identity

Trade Name
APL2002/1 Set mit Anstechdorn EUDAMED
Model / Reference
Infusionsset EUDAMED
52011 EUDAMED

Identifiers

Primary DI / UDI-DI
04042301080783 EUDAMED
Basic UDI-DI
4042301A0304AAGG EUDAMED
Direct Marketing DI
04042301080783 EUDAMED
EMDN Code
A03040199 INFUSION KITS (WITH OR W/O PUMP), SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

APL2002/1 Set mit Anstechdorn by PFM medical mepro GmbH — 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
DE-MF-000005190

Sources (1)

  • EUDAMED 5f786484-e69b-4b3c-8c7b-53ce6778617e 61 fields · synced Jun 19, 2026