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Rexeed

EUDAMED

Class IIb (EU MDR)

Ref SREXEED21AModel REXEED-21ARef 60SREXEED21AM

by Asahi Kasei Medical Co., Ltd.

Identity

Trade Name
REXEED EUDAMED
Device Name
ASAHI REXEED-A SERIES DIALYZER EUDAMED
Model / Reference
REXEED-21A EUDAMED
SREXEED21A EUDAMED
60SREXEED21AM EUDAMED

Identifiers

Primary DI / UDI-DI
04537693003873 EUDAMED
Basic UDI-DI
B-04537693003873 EUDAMED
4537693REX-A/0017C 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

Rexeed by Asahi Kasei Medical Co., Ltd. — Class IIb — MDR, MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
JP-MF-000013951
Authorised Representative
Asahi Kasei Medical Europe GmbH DE-AR-000012752

Sources (2)

  • EUDAMED 570cedda-d3d0-418e-b189-f49a78e115b3 61 fields · synced Oct 7, 2026
  • EUDAMED 8776e6f4-8939-44b2-b38d-9ad14715ede0 61 fields · synced May 16, 2026