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Medilen

EUDAMED

Class IIa (EU MDR)

Ref 3630022Model Blood line Set for haemodialysis (Pre-Pump and Post-Pump)

by Global Medikit Limited

Identity

Trade Name
Medilen EUDAMED
Device Name
Blood line Set for haemodialysis EUDAMED
Model / Reference
Blood line Set for haemodialysis (Pre-Pump and Post-Pump) EUDAMED
3630022 EUDAMED

Identifiers

Primary DI / UDI-DI
08903545081522 EUDAMED
Basic UDI-DI
8903545GMLBLH005ED EUDAMED
EMDN Code
F020180 ARTERIOVENOUS DIALYSIS LINES FOR HAEMODIALYSIS - HAEMOFILTRATION -HAEMODIAFILTRATION - ACCESSORIES EUDAMED

Classification

Device Class
Class IIa 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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Medilen by Global Medikit Limited — 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
IN-MF-000013635
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED cd9f7b4f-7169-4df7-b3ac-80f411238aaf 61 fields · synced Oct 5, 2026