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Rexeed

EUDAMED

Class IIb (EU MDR)

Ref 60SREXEED18AMRef SREXEED18AModel REXEED-18A

by Asahi Kasei Medical Co., Ltd.

Identity

Trade Name
REXEED EUDAMED
Device Name
ASAHI REXEED-A SERIES DIALYZER EUDAMED
Model / Reference
60SREXEED18AM EUDAMED
REXEED-18A EUDAMED
SREXEED18A EUDAMED

Identifiers

Primary DI / UDI-DI
04537693003866 EUDAMED
Basic UDI-DI
4537693REX-A/0017C EUDAMED
B-04537693003866 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 — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

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Manufacturer

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

Sources (2)

  • EUDAMED 99430e90-1caf-4c45-8990-d57edb8017f8 61 fields · synced Jun 9, 2026
  • EUDAMED b331d259-31aa-4990-b7a6-6c7153b40b41 61 fields · synced May 17, 2026