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Hollow Fiber Haemodiafilter

EUDAMED

Class IIb (EU MDR)

Ref SC023Model HDF15, HDF16, HDF17, HDF18, HDF19, HDF20, HDF21, HDF22, HDF23

by Shandong Weigao Blood Purification Products Co., Ltd.

Identity

Trade Name
Hollow Fiber Haemodiafilter EUDAMED
Device Name
Hollow Fiber Haemodiafilter EUDAMED
Model / Reference
HDF15, HDF16, HDF17, HDF18, HDF19, HDF20, HDF21, HDF22, HDF23 EUDAMED
SC023 EUDAMED

Identifiers

Primary DI / UDI-DI
56947793303781 EUDAMED
Basic UDI-DI
69477933HaemodiafilterN3 EUDAMED
Unit of Use DI
06947793303786 EUDAMED
EMDN Code
F01060303 DIALYSERS - UFC > 35 ml/h/mmHg, SYNTHETIC MEMBRANES EUDAMED

Classification

Device Class
Class IIb 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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Hollow Fiber Haemodiafilter by Shandong Weigao Blood Purification Products Co., Ltd. — Class IIb — 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
CN-MF-000012203
Authorised Representative
MedNet EC-REP C IIb GmbH DE-AR-000011194

Sources (1)

  • EUDAMED 7bdf3b3f-3e1d-4a02-99cc-ef1093593e63 61 fields · synced Oct 6, 2026