ALIAXIN SR - Indonesia BPOM Medical Device Registration
ALIAXIN SR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602220009. The device is manufactured by ROSE PHARMA SA from Switzerland, and is classified as Risk Class Kelas Resiko : D. 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 : 3
Manufacturer
ROSE PHARMA SACountry of Origin
Switzerland
Authorized Representative
PHARMINDO LESTARI AWARDAR Address
Jl. Boulevard BGR No. 1, Komplek Pergudangan BGR Gudang M, Kel. Kelapa Gading Barat, Kec. Kelapa Gading, Jakarta Utara, DKI Jakarta
Registration Date
Jan 24, 2022
Expiry Date
Dec 09, 2026
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
CELETEQUE Dermoscience Restorative Gel
FIDIA FARMACEUTICI S.P.A
GC INITIAL IQ ONE SQIN
KLEMA DENTALPRODUKTE GMBH
CELETEQUE Dermoscience Restorative Post Peel 30 g gel
FIDIA FARMACEUTICI S.P.A.
PROSPEC-PLUS Toothbrush
GC CORPORATION
GC Initial Lisi
KLEMA DENTALPRODUKTE GMBH
BURNAZIN Plus 25g cream
FIDIA FARMACEUTICI S.P.A.
EXACLEAR
GC CORPORATION FUJI OYAMA FACTORY
GC Gold Label HYBRID
GC CORPORATION FUJI OYAMA FACTORY
CERASMART270
GC DENTAL PRODUCTS CORPORATION
EQUIA Forte Coat
GC DENTAL PRODUCTS CORPORATION