Aqua Pure - Indonesia BPOM Medical Device Registration
Aqua Pure is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204420417. 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 PT. ALFA INTERNAL OPTINDO.
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
AVIZOR S.A.Country of Origin
Spain
Authorized Representative
PT. ALFA INTERNAL OPTINDOAR Address
JALAN KAREL SATSUIT TUBUN NOMOR 72 LANTAI 1 RT.001 / RW.001
Registration Date
Sep 02, 2024
Expiry Date
Feb 12, 2029
Product Type
Therapeutic Eye Equipment
Soft (hydrophilic) contact lens care products.
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