MIKROZID AF Liquid - Indonesia BPOM Medical Device Registration
MIKROZID AF Liquid is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903210472. The device is manufactured by SCHULKE & MAYR GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DEMKA SAKTI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SCHULKE & MAYR GMBH.Country of Origin
Germany
Authorized Representative
PT. DEMKA SAKTIAR Address
Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat
Registration Date
Jul 14, 2022
Expiry Date
Mar 18, 2027
Product Type
General Hospital Equipment and Other Individuals
Liquid chemical sterilants/high level disinfectants.
Non Electromedic Non Sterile
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