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CONNETTIVINA cerotto HI TECH

EUDAMED

Class IIa (EU MDR)

Ref 10000306Model AQC1-01-02C

by Fidia Farmaceutici S.p.A.

Identity

Trade Name
CONNETTIVINA cerotto HI TECH EUDAMED
Device Name
CONNETTIVINA cerotto HI TECH EUDAMED
Model / Reference
AQC1-01-02C EUDAMED
10000306 EUDAMED

Identifiers

Primary DI / UDI-DI
D-100003062U EUDAMED
Basic UDI-DI
B-100003062U EUDAMED
EMDN Code
M0599 MEDICAL PLASTERS - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

CONNETTIVINA cerotto HI TECH by Fidia Farmaceutici S.p.A. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
IT-MF-000026988

Sources (1)

  • EUDAMED 5807a075-49ea-451b-aa5b-eb5fefb0a969 61 fields · synced Jun 19, 2026