INSTAR S1 with Lidocaine - Indonesia BPOM Medical Device Registration
INSTAR S1 with Lidocaine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320188. The device is manufactured by BIOPLUS CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. SUCCESS WITH DAVID.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
BIOPLUS CO., LTDCountry of Origin
Korea
Authorized Representative
PT. SUCCESS WITH DAVIDAR Address
Gedung Nucira Lt. 3, Jl. MT. Haryono Kav. 27, Tebet Timur, Tebet
Registration Date
Apr 27, 2023
Expiry Date
Aug 21, 2025
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
LUMIGLAM S
LUMIGLAM H
REMEDIUM PLUS SUB-Q
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MIFILL Volume Plus Lidocaine
MIFILL Light Plus
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MCURE AQUAPEN2
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MINERVA PDO Suture
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DR. CANNULA
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INSTAR S2 with Lidocaine
BIOPLUS CO., LTD
INSTAR S3 with Lidocaine
BIOPLUS CO., LTD

