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LABORATOIRE L'IDEAL Parisien Sp. z o.o.

PL-MF-000005402 · Poland · Niegoszowice

LABORATOIRE L'IDEAL Parisien Sp. z o.o. is registered in the European database on medical devices as a manufacturer, with 106 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa86
Class IIb20

Most frequent device types declared: BUTIRECT Rectal suppositories Blister pack of 5 pieces in a carton wit, DEBUTIR Rectal suppositories, 10 suppositories in carton with instruct, DOZ MED BLISILUM Silikonowy żel na blizny 20ml tube in a single carto, Globulki dopochwowe w kartoniku jednostkowym wraz z instrukcją użycia, MedCare Advanced Scar Gel 20ml tube in a carton with instructions for .

Devices declared under this manufacturer

Showing 12 of 106 declared devices.

Catalogue references include AFTINEX Ulcer Gel packaged in a 10ml tube in a carton with instructio, DEBUTIR Rectal suppositories, 10 suppositories in carton with instruct, DOZ MED BLISILUM Silikonowy żel na blizny 20ml tube in a carton with , DOZ MED LINUMCARE 50g, JASNUM COMFORT 2 sztuk globulek w kartoniku jednostkowym wraz z instru, PROBUTIN Rectal suppositories Blister pack of 10 pieces in a carton wi.

European nomenclature codes declared: U089005, G05, U0803, M9002, V9099, V9017.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED106
Country of registrationPoland

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

Device-level evidence

Devices with a numeric GTIN103
Found in the U.S. device database0
Share0.0 %

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. LABORATOIRE L'IDEAL Parisien Sp. z o.o. was not found in either the U.S. or the Canadian register.

Notified body certificates

CertificateStatusExpiry
HZ 1554323-1issued2031-04-14

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