← Back to catalogue

APL2002/9 Set mit Anstechdorn u. 1, 2 Fil

EUDAMED

Class IIa (EU MDR)

Ref 52019Model Infusionsset

by PFM medical mepro GmbH

Identity

Trade Name
APL2002/9 Set mit Anstechdorn u. 1,2 Fil EUDAMED
Model / Reference
Infusionsset EUDAMED
52019 EUDAMED

Identifiers

Primary DI / UDI-DI
04042301081872 EUDAMED
Basic UDI-DI
4042301A0304AAGG EUDAMED
Direct Marketing DI
04042301081872 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

APL2002/9 Set mit Anstechdorn u. 1, 2 Fil 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000005190

Sources (1)

  • EUDAMED 1557d5e0-f6d2-4b42-ace5-edf977b69330 61 fields · synced Jul 27, 2026