OMNI Knife - Indonesia BPOM Medical Device Registration
OMNI Knife is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203718026. The device is manufactured by OMNI LENS PVT., LTD. from India, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PERFECT SINGLE OPTICS.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
OMNI LENS PVT., LTD.Country of Origin
India
Authorized Representative
PERFECT SINGLE OPTICSAR Address
Jl. Pintu Air Raya No. 36 KL. Pasar baru
Registration Date
Sep 15, 2021
Expiry Date
Jul 27, 2026
Product Type
Surgical Eye Equipment
Manual ophthalmic surgical instrument.
Non Electromedic Sterile
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