JUVEDERM VOLIFT with Lidocaine - Indonesia BPOM Medical Device Registration
JUVEDERM VOLIFT with Lidocaine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602812482. The device is manufactured by ALLERGAN from France, 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
ALLERGANCountry of Origin
France
Authorized Representative
PT. PHARMINDO LESTARI AWARDAR Address
Jl. Boulevard BGR No. 1, Komplek Pergudangan BGR Gudang M
Registration Date
Oct 23, 2024
Expiry Date
Nov 09, 2027
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
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GC CORPORATION FUJI OYAMA FACTORY
PROFHILO STRUCTURA 4.5%
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GC DENTAL PRODUCTS CORPORATION
JUVEDERM Volbella with Lidocaine
ALLERGAN
JUVEDERM Ultra Plus XC
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JUVEDERM Likes
ALLERGAN
JUVEDERM VOLUMA with Lidocaine
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JUVEDERM VOLUX
ALLERGAN
HYAL SYSTEM 1.8%
FIDIA FARMACEUTICI S.P.A.
HYAL SYSTEM ACP
FIDIA FARMACEUTICI S.P.A.