AUROSIL 1500 - Indonesia BPOM Medical Device Registration
AUROSIL 1500 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31203127912. The device is manufactured by AUROLAB from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MAIN INDEPENDENT MEDEQ.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
AUROLABCountry of Origin
India
Authorized Representative
PT. MAIN INDEPENDENT MEDEQAR Address
Ruko Graha Mas Pemuda Blok AC-19 jL. Pemuda Blok AC-19 Jl. Pemuda Kel. Jati Kec. Pulo Gadung Jakarta Timur
Registration Date
Dec 16, 2021
Expiry Date
Dec 03, 2025
Product Type
Surgical Eye Equipment
Intraocular fluid.
Non Electromedic Sterile
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