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Fevogel

EUDAMED

Class I (EU MDR)

Ref FG100140

by Pharmaplast

Identity

Trade Name
Fevogel EUDAMED
Device Name
Thermoregulating hydrogel EUDAMED
Model / Reference
FG100140 EUDAMED

Identifiers

Primary DI / UDI-DI
06221329007790 EUDAMED
Basic UDI-DI
62220238Fevocool8P EUDAMED
EMDN Code
M9001 CRYOTHERAPY AND THERMOTHERAPY DEVICES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland 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

Fevogel by Pharmaplast — 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

Manufacturer
Pharmaplast
EUDAMED SRN
EG-MF-000004501
Authorised Representative
E C REP LIMITED IE-AR-000003995

Sources (1)

  • EUDAMED 382c4723-748c-4d35-adfc-3fd1855e7400 61 fields · synced Jun 19, 2026