HUMAN MEDITEK PLASMA STERILIZER - Indonesia BPOM Medical Device Registration
HUMAN MEDITEK PLASMA STERILIZER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903020186. The device is manufactured by HUMAN MEDITEK CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEGA GLOBAL PRATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HUMAN MEDITEK CO., LTD.Country of Origin
Korea
Authorized Representative
PT. MEGA GLOBAL PRATAMAAR Address
JL. Cengkeh Blok 16 No. 11 Kel. Pinangsia Kec. Tamansari Jakarta Barat 11110
Registration Date
May 14, 2024
Expiry Date
Feb 15, 2027
Product Type
General Hospital Equipment and Other Individuals
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