G BOND - Indonesia BPOM Medical Device Registration
G BOND is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602220403. The device is manufactured by GC CORPORATION, FUJI OYAMA FACTORY from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PHARMINDO LESTARI AWARD.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GC CORPORATION, FUJI OYAMA FACTORYCountry of Origin
Japan
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
Dec 16, 2022
Expiry Date
Oct 14, 2026
Product Type
Prosthetic Dental Equipment
Dental cement.
Non Electromedic Non Sterile
GC Initial Lisi Block
GC Gold Label I Capsule
GC Gold Label VII EP CAPSULE
GC Gold Label PLUS CAPSULE
GC Gold Label VII CAPSULE
GC Gold Label II LC CAPSULE
GC Fuji IX (Atraumatic Restorative Treatment)
GC Gold Label Light-cured Universal Restorative 2 LC
GC Gold Label 1
GC Elite Cement 100
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
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JUVEDERM VOLUMA with Lidocaine
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JUVEDERM Likes
ALLERGAN
HYAL SYSTEM 1.8%
FIDIA FARMACEUTICI S.P.A.