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UDI Compass

Skinitril kožní roztok na fibromy, moluska, kondylomata

Certificate valid

Snapshot 2026-11-02 · Link to EUDAMED

UDI-DI 08594071270711Basic UDI-DI 859407127SKIT3

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Class IIa · MDR · ENEO Pharmaceuticals s. r. o.

Identification

Model
—
EMDN
V0999
Issuing agency
GS1
Device status
active
Sterile
No
Implantable
No
Measuring function
No
Reusable surgical
No

Certificates

2026-MDR/QS-056

EU quality management system · valid

Notified body: 3EC International a.s. (2265)

Valid from 2026-08-07 · Expiry 2027-12-09

Scope not stated in certificate data.

Certificate’s own scope text — not a compliance opinion from UDI Compass.

Manufacturer

ENEO Pharmaceuticals s. r. o.

SRN CZ-MF-000017906

CZ · Stříbrná Skalice

manufacturer

Related UDI-DIs

No other UDI-DIs share this Basic UDI-DI in this snapshot.

All UDI-DIs in this Basic UDI-DI family

Canonical device page: /device/skinitril-kozni-roztok-na-fibromy-moluska-kondylomata-0711 · UDI page: /udi/08594071270711

All devices from ENEO Pharmaceuticals s. r. o.