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Zώνειες Αιμοληψίας

EUDAMED

Class I (EU MDR)

Ref FN-TNQ030201Model FN-TNQ03

by Finess Healthcare Group Co., Ltd

Identity

Trade Name
Zώνειες αιμοληψίας EUDAMED
Device Name
Tourniquet EUDAMED
Model / Reference
FN-TNQ03 EUDAMED
FN-TNQ030201 EUDAMED

Identifiers

Primary DI / UDI-DI
16973911696994 EUDAMED
Basic UDI-DI
697391169TNQ03T5 EUDAMED
EMDN Code
V9003 TOURNIQUETS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Greece 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

Category: Limb tourniquet, manual, reusable

Zώνειες Αιμοληψίας by Finess Healthcare Group Co., Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Limb tourniquet, manual, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000004124
Authorised Representative
Zoustech S.L. ES-AR-000002008

Sources (1)

  • EUDAMED ea9fc2f8-e58d-4712-b319-c008426f6a94 61 fields · synced Jun 19, 2026