OMNIVISC 2% - Indonesia BPOM Medical Device Registration
OMNIVISC 2% is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31203717971. The device is manufactured by OMNI LENS PVT. LTD. from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. PERFECT SINGLE OPTICS.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
OMNI LENS PVT. LTD.Country of Origin
India
Authorized Representative
PT. PERFECT SINGLE OPTICSAR Address
Jl. Pintu Air Raya No. 36 KL. Pasar baru
Registration Date
Oct 26, 2021
Expiry Date
Jul 24, 2026
Product Type
Surgical Eye Equipment
Intraocular fluid.
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