FOCUS 8/0 PGA - Indonesia BPOM Medical Device Registration
FOCUS 8/0 PGA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203520006. The device is manufactured by AUROLAB from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KHASANAH ALKESINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AUROLABCountry of Origin
India
Authorized Representative
PT. KHASANAH ALKESINDOAR Address
Jl. Prof. Dr. Soepomo SH, No.178 A Royal Palace B 39. RT. 001 RW. 015, Prov. DKI Jakarta, Kota Jakarta Selatan, Kec. Tebet, Kel. Menteng Dalam
Registration Date
Jan 13, 2025
Expiry Date
Jan 01, 2028
Product Type
Surgical Eye Equipment
Suture, Absorbable, Ophthalmic
Non Electromedic Sterile
ROHTO Visc
FOCUS 10/0 Nylon
AUROFLEX
I-VISION Hydrophilic Foldable Poly Hydroxy Ethyl Methacrylate IOL
AUROVISC Hypermellose Ophthalmic Solution
KALVIOL Hydrophilic Aspheric
ROHTO T-BLUE
HUMMINGBIRD Phacoemulsifier
Auro Octane
KALVIS Hypromellose Ophthalmic Solution USP 2% w/v
PRECIZON GO
OPHTEC B.V
FOCUS 10/0 Nylon
AUROLAB
ARTISAN Myopia
OPHTEC B.V.
ARTISAN Aphakia
OPHTEC B.V.
OPHTEC Enclavation Needle
OPHTEC B.V.
ARTISAN Toric
OPHTEC B.V.
ARTIFLEX Toric
OPHTEC B.V.
ARTIFLEX Myopia
OPHTEC B.V.
CATAGEL Plus Sodium Hyaluronate Ophthalmic Solution - 1.8%w/v
OPHTHALMIC TECHNOLOGY
CATAGEL Hydroxypropyl Methylcellulose Ophthalmic Solution-2%w/v
OPHTHALMIC TECHNOLOGY