STYLAGE Hydromax - Indonesia BPOM Medical Device Registration
STYLAGE Hydromax is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602420017. The device is manufactured by VIVACY LABORATORIES from France, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. FONDA MEDIKA MAIN.
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 : 3
Manufacturer
VIVACY LABORATORIESCountry of Origin
France
Authorized Representative
PT. FONDA MEDIKA MAINAR Address
Komplek Roxy Mas Blok C-4 No 1-2 Lt.2 Jl. KH Hasyim Ashari No. 125
Registration Date
Feb 06, 2024
Expiry Date
Dec 16, 2027
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
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