← Back to catalogue

Fevogel

EUDAMED

Class I (EU MDR)

Ref FG50140Ref FG40110Ref FG50120

by Pharmaplast

Identity

Trade Name
Fevogel EUDAMED
Device Name
Thermoregulating hydrogel EUDAMED
Model / Reference
FG50140 EUDAMED
FG40110 EUDAMED
FG50120 EUDAMED

Identifiers

Primary DI / UDI-DI
06221329007806 EUDAMED
06221329007776 EUDAMED
06221329007783 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (3)

  • EUDAMED 210f272e-6212-450a-9bcc-f88e916602e7 61 fields · synced Aug 4, 2026
  • EUDAMED 1c671229-31c0-489e-9e88-46c04bb498c2 61 fields · synced May 18, 2026
  • EUDAMED 1d726162-9bb6-47fe-a82e-2528556b6aef 61 fields · synced May 18, 2026