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Imutis IBS 30 cpr BE

EUDAMED

Class IIb (EU MDR)

Ref FTP091

by Labomar S.p.A.

Identity

Trade Name
Imutis IBS 30 cpr BE EUDAMED
Device Name
SMILEUM EUDAMED
Model / Reference
FTP091 EUDAMED

Identifiers

Primary DI / UDI-DI
D-FTP091_2KC EUDAMED
Basic UDI-DI
B-FTP091_2KC EUDAMED
EMDN Code
G0401 ORALLY ADMINISTERED DEVICES FOR THE THERAPY OF GASTRO-INTESTINAL DISORDERS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Belgium 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

Imutis IBS 30 cpr BE by Labomar S.p.A. — Class IIb — 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

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

Sources (1)

  • EUDAMED 16055907-d0bd-424a-9107-6c41e4d742d9 61 fields · synced Jun 20, 2026