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Bei Reizdarm DE, AU

EUDAMED

Class IIb (EU MDR)

Ref FTP054

by Labomar S.p.A.

Identity

Trade Name
Bei Reizdarm DE, AU EUDAMED
Device Name
NORMOBOWELL COMPRESSE I.B.S. EUDAMED
Model / Reference
FTP054 EUDAMED

Identifiers

Primary DI / UDI-DI
D-FTP054EU EUDAMED
Basic UDI-DI
B-FTP054EU EUDAMED
EMDN Code
G0401 ORALLY ADMINISTERED DEVICES FOR THE THERAPY OF GASTRO-INTESTINAL DISORDERS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany 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

Bei Reizdarm DE, AU 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 2bd0cf34-e58f-4301-af5d-781581d4441c 61 fields · synced Jul 18, 2026