RESTYLANE Kissing - Indonesia BPOM Medical Device Registration
RESTYLANE Kissing is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320307. The device is manufactured by Q-MED AB from Sweden, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. 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.
RESTYLANE Kysse
Risk Classification
Product Class
Kelas : 3
Manufacturer
Q-MED ABCountry of Origin
Sweden
Authorized Representative
PT. 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
Aug 13, 2024
Expiry Date
Dec 31, 2026
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
RESTYLANE Refyne
RESTYLANE Volyme
RESTYLANE LYFT LIDOCAINE
RESTYLANE Skinboosters Vital Light Lidocaine
RESTYLANE Defyne
RESTYLANE Lidocaine
RESTYLANE Skinboosters Vital Lidocaine
RESTYLANE Skinboosters Vital Light Lidocaine
GC Tooth Mousse Milkshake
GC CORPORATION FUJI OYAMA FACTORY
PROFHILO STRUCTURA 4.5%
IBSA FARMACEUTICI ITALIA SRL
G-AENIAL Universal Flo
GC DENTAL PRODUCTS CORPORATION
JUVEDERM VOLUX
ALLERGAN
JUVEDERM Likes
ALLERGAN
JUVEDERM VOLUMA with Lidocaine
ALLERGAN
JUVEDERM VOLIFT with Lidocaine
ALLERGAN
JUVEDERM Volbella with Lidocaine
ALLERGAN
JUVEDERM Ultra Plus XC
ALLERGAN
HYAL SYSTEM 1.8%
FIDIA FARMACEUTICI S.P.A.