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 21204126616. The device is manufactured by CIBA VISION ASIAN MANUFACTURING AND LOGISTICS PTE LTD. from Singapore, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GRACE ARGON MEDICA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Country of Origin
Singapore
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
Aug 01, 2024
Expiry Date
Mar 31, 2027
Product Type
Therapeutic Eye Equipment
Soft (hydrophilic) contact lens.
Non Electromedic Sterile
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PRECISION 1 ™
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