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Tournistretch 25 Single Patient

EUDAMED

Class I (EU MDR)

Ref 43451TPEOS/ASEP25Model Tournistretch

by Asep Healthcare Ltd

Identity

Trade Name
Tournistretch 25 Single Patient EUDAMED
Device Name
Tournistretch EUDAMED
Model / Reference
Tournistretch EUDAMED
43451TPEOS/ASEP25 EUDAMED

Identifiers

Primary DI / UDI-DI
05060728810331 EUDAMED
Basic UDI-DI
506072881MDTF002CS EUDAMED
Direct Marketing DI
05060728810331 EUDAMED
EMDN Code
V9003 TOURNIQUETS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium 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

Tournistretch 25 Single Patient by Asep Healthcare 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

Manufacturer
Asep Healthcare Ltd
EUDAMED SRN
GB-MF-000016192
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED e3e718f0-6ea7-41ed-862b-7cd6286ee0c7 61 fields · synced Jun 19, 2026