MEDIZAR HAND FOAM SANITISER - Indonesia BPOM Medical Device Registration
MEDIZAR HAND FOAM SANITISER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903913548. The device is manufactured by MEDIZAR SANITISER PRODUCTS LIMITED from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEGAH MEDIKA PHARMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MEDIZAR SANITISER PRODUCTS LIMITEDCountry of Origin
United Kingdom
Authorized Representative
PT. MEGAH MEDIKA PHARMAAR Address
Jl. Minangkabau Timur Raya No. 07 RT 006 RW 008
Registration Date
Dec 13, 2019
Expiry Date
Oct 30, 2024
Product Type
General Hospital Equipment and Other Individuals
Liquid chemical sterilants/high level disinfectants.
Non Electromedic Non Sterile
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