← Back to catalogue

Anginetten Hals & Husten Sirup 120 mL DE

EUDAMED

Class IIa (EU MDR)

Ref FTPR109

by Labomar S.p.A.

Identity

Trade Name
Anginetten Hals & Husten Sirup 120 mL DE EUDAMED
Anginetten Hals & Husten Sirup 100 mL DE EUDAMED
Device Name
LongAct syrup EUDAMED
Model / Reference
FTPR109 EUDAMED

Identifiers

Primary DI / UDI-DI
08056300620969 EUDAMED
Basic UDI-DI
805630062FTPR109E3 EUDAMED
EMDN Code
V9017 ORAL ADMINISTRATION PREPARATIONS NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Anginetten Hals & Husten Sirup 120 mL DE by Labomar S.p.A. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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 5c60a410-7e16-48f6-9d17-5d6fac56aa0a 61 fields · synced Jul 9, 2026
  • EUDAMED 5417785a-aefc-4392-b4a8-7400ad54bbba 61 fields · synced Jul 9, 2026