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Cerezen System

EUDAMED

Class IIa (EU MDR)

Ref 22203

by Renew Group Private Limited

Identity

Device Name
Cerezen System EUDAMED
Model / Reference
22203 EUDAMED

Identifiers

Primary DI / UDI-DI
08885021530000 EUDAMED
Basic UDI-DI
888502153CerezenW2 EUDAMED
Direct Marketing DI
08885021530000 EUDAMED
EMDN Code
Z120607 PNEUMATIC COMPRESSION EQUIPMENT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Ireland EUDAMED

Clinical & Handling

Sterile

No

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

Cerezen System by Renew Group Private 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
SG-MF-000049528
Authorised Representative
Renew Health Ltd. IE-AR-000013707

Sources (1)

  • EUDAMED 8646c86b-9032-4285-9d28-77a290e5d5eb 61 fields · synced Jul 29, 2026