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Rheofilter

EUDAMED

Class IIb (EU MDR)

Ref 60SXR4000Model XR-4000

by Asahi Kasei Medical Co., Ltd.

Identity

Trade Name
Rheofilter EUDAMED
Device Name
Rheofilter XR EUDAMED
Model / Reference
XR-4000 EUDAMED
60SXR4000 EUDAMED

Identifiers

Primary DI / UDI-DI
04537693007116 EUDAMED
Basic UDI-DI
4537693RF-XR/0018J EUDAMED
EMDN Code
B030203 SINGLE PLASMA COMPONENTS REMOVAL DEVICES AND KITS 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

Rheofilter by Asahi Kasei Medical 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
JP-MF-000013951
Authorised Representative
Asahi Kasei Medical Europe GmbH DE-AR-000012752

Sources (1)

  • EUDAMED 1932ca1c-1a8e-4a92-8dfc-63c831bb98fd 61 fields · synced Jun 19, 2026