CELETEQUE Dermoscience Restorative Post Peel 30 g gel - Indonesia BPOM Medical Device Registration
CELETEQUE Dermoscience Restorative Post Peel 30 g gel is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603020199. 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.A.Country of Origin
Italy
Authorized Representative
PHARMINDO LESTARI AWARDAR Address
Jl. Boulevard BGR No. 1, Komplek Pergudangan BGR Gudang M
Registration Date
Sep 17, 2024
Expiry Date
Feb 20, 2029
Product Type
Surgical Equipment
Hydrogel wound dressing and burn dressing.
Non Electromedic Non Sterile
CELETEQUE Dermoscience Restorative Gel
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