MENICARE Plus Multipurpose Solution - Indonesia BPOM Medical Device Registration
MENICARE Plus Multipurpose Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204515870. The device is manufactured by MENICON PHARMA S.A.S. from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ALFA INTERNAL OPTINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MENICON PHARMA S.A.S.Country of Origin
France
Authorized Representative
PT. ALFA INTERNAL OPTINDOAR Address
JALAN KAREL SATSUIT TUBUN NOMOR 72 LANTAI 1 RT.001 / RW.001
Registration Date
Jun 21, 2024
Expiry Date
Dec 31, 2026
Product Type
Therapeutic Eye Equipment
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