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CuffMed F1

EUDAMED

Class IIa (EU MDR)

Ref 03Model CuffMed F1

by Good Medica Spółka z ograniczoną odpowiedzialnością

Identity

Trade Name
CuffMed F1 EUDAMED
Model / Reference
CuffMed F1 EUDAMED
03 EUDAMED

Identifiers

Primary DI / UDI-DI
05901085023012 EUDAMED
Basic UDI-DI
5901085023CUFFMEDBR EUDAMED
EMDN Code
V9003 TOURNIQUETS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Poland 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Limb tourniquet, manual, reusable

CuffMed F1 by Good Medica Spółka z ograniczoną odpowiedzialnością — Class IIa — 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
PL-MF-000027329

Sources (1)

  • EUDAMED 3d660d5e-296b-4e43-a7fd-d1c26da3da7e 61 fields · synced Jun 20, 2026