EU → North America Device Access

UNI-PHARMA KLEON TSETIS PHARMACEUTICAL LABORATORIES S.A.

GR-MF-000032960 · Greece · Athens

UNI-PHARMA KLEON TSETIS PHARMACEUTICAL LABORATORIES S.A. is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa4
Class IIb1

Devices declared under this manufacturer

Catalogue references include CURADERM POWDER SPRAY, INSTARET HERBAL, REPEL ANTI-LICE RESTORE, REPEL MYCOCLEAN, UNIBURN AFTER SUN.

European nomenclature codes declared: V9099, Q03040299, V901099, V901001.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED5
Country of registrationGreece

⚠️ Not found is not the same as not sold — how this comparison can be wrong.

Canadian market access

Health Canada licence listingNot found in the Canadian register

⚠️ Canada lists no Class I devices at all — what that excludes.

North American profile: Neither register. UNI-PHARMA KLEON TSETIS PHARMACEUTICAL LABORATORIES S.A. was not found in either the U.S. or the Canadian register.

Other manufacturers in Greece

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