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Bone Cement Delivery Cannula

EUDAMED

Class IIa (EU MDR)

Ref SV102-0301301401Model SV102-0301351801, SV102-0302351801, SV102-0303351801, SV102-0301351401, SV102-0302351401, SV102-0303351401, SV102-0301301801, SV102-0302301801, SV102-0303301801, SV102-0301301401, SV102-0302301401, SV102-0303301401

by Hicren (Zhejiang) Medtech Co., Ltd.

Identity

Device Name
Bone Cement Delivery Cannula EUDAMED
Model / Reference
SV102-0301351801, SV102-0302351801, SV102-0303351801, SV102-0301351401, SV102-0302351401, SV102-0303351401, SV102-0301301801, SV102-0302301801, SV102-0303301801, SV102-0301301401, SV102-0302301401, SV102-0303301401 EUDAMED
SV102-0301301401 EUDAMED

Identifiers

Primary DI / UDI-DI
06936260802532 EUDAMED
Basic UDI-DI
69362608SV102-03014R EUDAMED
EMDN Code
P099002 ORTHOPAEDIC CEMENT PREPARATION AND APPLICATION DEVICES AND KITS EUDAMED

Classification

Device Class
Class IIa 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

Bone Cement Delivery Cannula by Hicren (Zhejiang) Medtech Co., Ltd. — 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

Manufacturer
Hicren (Zhejiang) Medtech Co., Ltd.
EUDAMED SRN
CN-MF-000025999
Authorised Representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Sources (1)

  • EUDAMED fcfc8c3d-7343-417b-b051-30de807d03f4 61 fields · synced Jul 29, 2026