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DERMATOP patch HI TECH

EUDAMED

Class IIa (EU MDR)

Ref 10001150Model AQC1-03-01A

by Fidia Farmaceutici S.p.A.

Identity

Trade Name
DERMATOP patch HI TECH EUDAMED
Device Name
DERMATOP patch HI TECH EUDAMED
Model / Reference
AQC1-03-01A EUDAMED
10001150 EUDAMED

Identifiers

Primary DI / UDI-DI
D-100011502U EUDAMED
Basic UDI-DI
B-100011502U 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 908fd84a-0caf-4361-8846-b2dff9b16602 61 fields · synced Jun 19, 2026