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DERMATOP patch HI TECH

EUDAMED

Class IIa (EU MDR)

Ref 10001302Model AQC1-03-02B

by Fidia Farmaceutici S.p.A.

Identity

Trade Name
DERMATOP patch HI TECH EUDAMED
Device Name
DERMATOP patch HI TECH EUDAMED
Model / Reference
AQC1-03-02B EUDAMED
10001302 EUDAMED

Identifiers

Primary DI / UDI-DI
D-100013022T EUDAMED
Basic UDI-DI
B-100013022T EUDAMED
EMDN Code
M0599 MEDICAL PLASTERS - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Czechia 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

DERMATOP patch 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 48dc9e76-f876-42a7-9f49-dd95af4f6c36 61 fields · synced Jul 29, 2026