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Radilock™

EUDAMED

Class I (EU MDR)

Ref 176I22Model Type I

by APT Medical Inc.

Identity

Trade Name
Radilock™ EUDAMED
Device Name
Radilock™ Radial Compression Device EUDAMED
Model / Reference
Type I EUDAMED
176I22 EUDAMED

Identifiers

Primary DI / UDI-DI
06931896185691 EUDAMED
Basic UDI-DI
69318961ZXD011768C EUDAMED
EMDN Code
V9003 TOURNIQUETS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

Category: Limb tourniquet, manual, reusable

Radilock™ by APT Medical Inc. — 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
APT Medical Inc.
EUDAMED SRN
CN-MF-000009046
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED ebc8bbf5-c0d6-49c1-9290-ff250e0e3d80 61 fields · synced Jun 17, 2026