BIOCLEAR Multi-Purpose Solution with HPMC - Indonesia BPOM Medical Device Registration
BIOCLEAR Multi-Purpose Solution with HPMC is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204918467. The device is manufactured by FORTIS MEDI PHARMACEUTICAL, INC. from Philippines, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GELFLEX VISION INDONESIA.
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
Manufacturer
FORTIS MEDI PHARMACEUTICAL, INC.Country of Origin
Philippines
Authorized Representative
PT. GELFLEX VISION INDONESIAAR Address
JL. AM. SANGAJI NO 17 RT.009/RW.007
Registration Date
Dec 20, 2019
Expiry Date
Oct 21, 2024
Product Type
Therapeutic Eye Equipment
Soft (hydrophilic) contact lens care products.
Non Electromedic Sterile

