SILICONE 1000 - Indonesia BPOM Medical Device Registration
SILICONE 1000 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31204819534. The device is manufactured by ALCON RESEARCH, LLC. from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is BINASUKSES CANTEEN.
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SILIKON 1000
Risk Classification
Product Class
Kelas : 3
Manufacturer
ALCON RESEARCH, LLC.Country of Origin
United States
Authorized Representative
BINASUKSES CANTEENAR Address
JL. PULO KAMBING II NO.26 KAWASAN INDUSTRI PULOGADUNG
Registration Date
Feb 22, 2023
Expiry Date
Jul 01, 2026
Product Type
Therapeutic Eye Equipment
Intraocular fluid.
Non Electromedic Sterile
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