RESTYLANE Skinboosters Vital Light Lidocaine - Indonesia BPOM Medical Device Registration
RESTYLANE Skinboosters Vital Light Lidocaine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320311. 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.
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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
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RESTYLANE LYFT LIDOCAINE
RESTYLANE Defyne
RESTYLANE Skinboosters Vital Lidocaine
RESTYLANE Lidocaine
RESTYLANE Skinboosters Vital Light Lidocaine
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HYAL SYSTEM 1.8%
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