AVIZOR Enzyme - Indonesia BPOM Medical Device Registration
AVIZOR Enzyme is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204705505. The device is manufactured by AVIZOR S.A. from Spain, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ALFA INTERNAL OPTINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AVIZOR S.A.Country of Origin
Spain
Authorized Representative
ALFA INTERNAL OPTINDOAR Address
Jl. Melawai Raya No. 67-68
Registration Date
Jan 12, 2022
Expiry Date
Jun 24, 2025
Product Type
Therapeutic Eye Equipment
Soft (hydrophilic) contact lens care products.
Non Electromedic Sterile
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