CELETEQUE Dermoscience Restorative Gel - Indonesia BPOM Medical Device Registration
CELETEQUE Dermoscience Restorative Gel is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603520180. The device is manufactured by FIDIA FARMACEUTICI S.P.A from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PHARMINDO LESTARI AWARD.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
FIDIA FARMACEUTICI S.P.ACountry of Origin
Italy
Authorized Representative
PHARMINDO LESTARI AWARDAR Address
World Trade Centre (WTC) 1 Building, Floor 15 JI. Jend. Sudirman Kav. 29 - 31, Jakarta 12920, Indonesia
Registration Date
Jan 19, 2025
Expiry Date
Aug 26, 2029
Product Type
Surgical Equipment
Hydrogel wound dressing and burn dressing.
Non Electromedic Non Sterile
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KLEMA DENTALPRODUKTE GMBH
CELETEQUE Dermoscience Restorative Post Peel 30 g gel
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