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Kältesofortkompresse

EUDAMED

Class I (EU MDR)

Ref L04900001

by Gello GmbH Geltechnik

Identity

Trade Name
Kältesofortkompresse EUDAMED
Device Name
Kältesofortkompresse EUDAMED
Model / Reference
L04900001 EUDAMED

Identifiers

Primary DI / UDI-DI
04251765100313 EUDAMED
Basic UDI-DI
42517651AG50FA EUDAMED
Direct Marketing DI
04251765100313 EUDAMED
EMDN Code
M9001 CRYOTHERAPY AND THERMOTHERAPY DEVICES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Kältesofortkompresse by Gello GmbH Geltechnik — 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
DE-MF-000010607

Sources (1)

  • EUDAMED 0be0f117-bc57-469d-a60e-ad1f64ebfd5b 61 fields · synced Jun 18, 2026