← Back to catalogue

Actirub Maux De Gorge Fr

EUDAMED

Class IIa (EU MDR)

Ref FTP088Ref FTPR88

by Labomar S.p.A.

Identity

Trade Name
ACTIRUB MAUX DE GORGE FR EUDAMED
Device Name
Icebalm EUDAMED
Model / Reference
FTP088 EUDAMED
FTPR88 EUDAMED

Identifiers

Primary DI / UDI-DI
D-FTP088_1L6 EUDAMED
08056300621393 EUDAMED
Basic UDI-DI
B-FTP088_1L6 EUDAMED
805630062FTPR88A8 EUDAMED
EMDN Code
V9017 ORAL ADMINISTRATION PREPARATIONS NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Actirub Maux De Gorge Fr by Labomar S.p.A. — Class IIa — MDR, MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (2)

  • EUDAMED 27223dd7-3384-4cae-8f3b-13ffd5e453d2 61 fields · synced Jul 18, 2026
  • EUDAMED 93a70e44-c8ed-463e-a0c4-03901e77580f 61 fields · synced May 18, 2026