PRECISION 1 - Indonesia BPOM Medical Device Registration
PRECISION 1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204420469. The device is manufactured by ALCON RESEARCH, LLC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GRACE ARGON MEDICA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ALCON RESEARCH, LLC.Country of Origin
United States
Authorized Representative
PT. GRACE ARGON MEDICAAR Address
Titan Center Lantai 4, Jl. Boulevard Bintaro Blok B7/B1 No. 5 Bintaro Jaya Sektor 7
Registration Date
Oct 15, 2024
Expiry Date
Mar 31, 2027
Product Type
Therapeutic Eye Equipment
Soft (hydrophilic) contact lens.
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