ERK-9000 Autorefractor/Keratometer - Indonesia BPOM Medical Device Registration
ERK-9000 Autorefractor/Keratometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201711691. The device is manufactured by U.S OPHTHALMIC LLC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PRIMARY WORKS.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
U.S OPHTHALMIC LLC.Country of Origin
United States
Authorized Representative
PT. PRIMARY WORKSAR Address
Daan Mogot Arcadia Blok F.1/8A-8B Jl. Daan Mogot Km 21, Kelurahan Batu Ceper
Registration Date
Mar 22, 2022
Expiry Date
Oct 28, 2025
Product Type
Diagnostic Eye Equipment
Ophthalmic refractometer.
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