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Jalosome Oral Barrier UK, IT, PT, TR, RO, ES, SE, DK, NO, FI, SK, CZ, HU

EUDAMED

Class IIa (EU MDR)

Ref FTP082

by Labomar S.p.A.

Identity

Trade Name
Jalosome Oral Barrier UK, IT, PT, TR, RO, ES, SE, DK, NO, FI, SK, CZ, HU EUDAMED
Device Name
MUCOSITI gel EUDAMED
Model / Reference
FTP082 EUDAMED

Identifiers

Primary DI / UDI-DI
D-FTP082EZ EUDAMED
Basic UDI-DI
B-FTP082EZ EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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

Category: Device sterilization/disinfection container, reusable

Jalosome Oral Barrier UK, IT, PT, TR, RO, ES, SE, DK, NO, FI, SK, CZ, HU by Labomar S.p.A. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Labomar S.p.A.
EUDAMED SRN
IT-MF-000007965

Sources (1)

  • EUDAMED d123148b-9063-4fc9-a9d4-25dc1dc72294 61 fields · synced Oct 6, 2026