ZYBIO H58 DN Diluent - Indonesia BPOM Medical Device Registration
ZYBIO H58 DN Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208420339. The device is manufactured by ZYBIO INC., from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ZYBIO MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ZYBIO INC.,Country of Origin
China
Authorized Representative
ZYBIO MEDICAL INDONESIAAR Address
Satrio Tower Unit 8, Lantai 14 No. 5 Bok C4, Jl. Prof. Dr, Satrio No. 7, Kel. Setiabudi, Kec. Kuningan Timur, Kota Jakarta Selatan, Prov. DKI Jakarta
Registration Date
Nov 01, 2024
Expiry Date
Jan 30, 2029
Product Type
Hematological Reagents
Blood cell diluents
Invitro Diagnostics
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