MENICON Z E-1 - Indonesia BPOM Medical Device Registration
MENICON Z E-1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204814439. The device is manufactured by MENICON CO. LTD, SEKI PLANT from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is 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
MENICON CO. LTD, SEKI PLANTCountry of Origin
Japan
Authorized Representative
ALFA INTERNAL OPTINDOAR Address
JALAN KAREL SATSUIT TUBUN NOMOR 72 LANTAI 1 RT.001 / RW.001
Registration Date
Jun 24, 2024
Expiry Date
Dec 31, 2026
Product Type
Therapeutic Eye Equipment
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