← Back to catalogue

Quixx Sore Throat 100 mL FI/SE

EUDAMED

Class IIa (EU MDR)

Ref FTPR107

by Labomar S.p.A.

Identity

Trade Name
Quixx Sore Throat 100 mL FI/SE EUDAMED
Quixx Sore Throat 100 mL FI, SE EUDAMED
Device Name
Quixx Sore Throat EUDAMED
Model / Reference
FTPR107 EUDAMED

Identifiers

Primary DI / UDI-DI
08056300620945 EUDAMED
Basic UDI-DI
805630062FTPR107DX EUDAMED
EMDN Code
V9017 ORAL ADMINISTRATION PREPARATIONS NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Finland 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

Quixx Sore Throat 100 mL FI/SE 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 ea149b69-fa17-46dc-bc08-5a967eaf4389 61 fields · synced Jul 28, 2026
  • EUDAMED d24dda13-b24e-404c-808b-851eaf328846 61 fields · synced Jul 28, 2026