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Cerotti Effetto Freddo

EUDAMED

Class I (EU MDR)

Ref CERFRE03DPModel CEROTTI EFFETTO FREDDO

by Bericah S.p.A.

Identity

Trade Name
CEROTTI EFFETTO FREDDO EUDAMED
Device Name
PATCH FREDDO EUDAMED
Model / Reference
CEROTTI EFFETTO FREDDO EUDAMED
CERFRE03DP EUDAMED

Identifiers

Primary DI / UDI-DI
08024151818378 EUDAMED
Basic UDI-DI
8024151CERFRE03DPAM EUDAMED
Direct Marketing DI
08024151818378 EUDAMED
EMDN Code
M9001 CRYOTHERAPY AND THERMOTHERAPY DEVICES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

Cerotti Effetto Freddo by Bericah S.p.A. — 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
Bericah S.p.A.
EUDAMED SRN
IT-MF-000007397

Sources (1)

  • EUDAMED e9d28a7a-6962-43c0-94a4-9699a527ad5e 61 fields · synced Jun 18, 2026