CRYSTAL FOLD - Indonesia BPOM Medical Device Registration
CRYSTAL FOLD is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202220004. The device is manufactured by BECOMES MEDITECH from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. OPTIMA GLOBAL INDONESIA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
BECOMES MEDITECHCountry of Origin
India
Authorized Representative
PT. OPTIMA GLOBAL INDONESIAAR Address
JL. Ciputat Raya No. 8 Perkantoran Pinang 8, RT 001 RW 006 Pondok Pinang , Kebayoran Lama Jakarta Selatan 12310
Registration Date
Jan 12, 2022
Expiry Date
Mar 31, 2026
Product Type
Prosthetic Eye Equipment
Intraocular lens.
Non Electromedic Sterile
