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Kompres Flex Sanity Standard (10 x 26 cm)

EUDAMED

Class I (EU MDR)

Ref 5907438901778Model Mini (10 x10 cm), Standard (10 x 26 cm), Medium (19 x 22 cm), Max (19 x 30 cm)

by Albert Polska Sp. z o.o.

Identity

Trade Name
Kompres Flex Sanity Standard (10 x 26 cm) EUDAMED
Device Name
Kompres Flex Sanity EUDAMED
Model / Reference
Mini (10 x10 cm), Standard (10 x 26 cm), Medium (19 x 22 cm), Max (19 x 30 cm) EUDAMED
5907438901778 EUDAMED

Identifiers

Primary DI / UDI-DI
05907438901778 EUDAMED
Basic UDI-DI
59074389104UU EUDAMED
Direct Marketing DI
05907438901778 EUDAMED
EMDN Code
M9001 CRYOTHERAPY AND THERMOTHERAPY DEVICES EUDAMED

Classification

Device Class
Class I 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

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Hot/cold therapy pack, reusable

Kompres Flex Sanity Standard (10 x 26 cm) by Albert Polska Sp. z o.o. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Hot/cold therapy pack, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
PL-MF-000007130

Sources (1)

  • EUDAMED 5840683a-c1bb-47cd-a16e-4732e082c824 61 fields · synced Jul 11, 2026