AUROSIL PLUS - Indonesia BPOM Medical Device Registration
AUROSIL PLUS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31203220038. 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
May 30, 2022
Expiry Date
Dec 03, 2025
Product Type
Surgical Eye Equipment
Intraocular fluid.
Non Electromedic Sterile
ROHTO Visc
FOCUS 8/0 PGA
FOCUS 10/0 Nylon
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AUROVISC Hypermellose Ophthalmic Solution
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