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Inflation Device

EUDAMED

Class I (EU MDR)

Ref SV240-30Model SV240-20, SV240-25, SV240-30, SV240-40

by Hicren (Zhejiang) Medtech Co., Ltd.

Identity

Device Name
Inflation Device EUDAMED
Model / Reference
SV240-20, SV240-25, SV240-30, SV240-40 EUDAMED
SV240-30 EUDAMED

Identifiers

Primary DI / UDI-DI
06936260800026 EUDAMED
Basic UDI-DI
69362608SV240S9 EUDAMED
EMDN Code
P099002 ORTHOPAEDIC CEMENT PREPARATION AND APPLICATION DEVICES AND KITS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain 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

Inflation Device by Hicren (Zhejiang) Medtech Co., Ltd. — Class I — 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-000025999
Authorised Representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Sources (1)

  • EUDAMED 3b05086f-ff80-4f5c-90a2-139881554df6 61 fields · synced Oct 6, 2026