BLESSMED Transcutaneous Jaundice Detector - Indonesia BPOM Medical Device Registration
BLESSMED Transcutaneous Jaundice Detector is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501313585. The device is manufactured by XUZHOU KEJIAN HI-TECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BLESINDO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
XUZHOU KEJIAN HI-TECH CO., LTD.Country of Origin
China
Authorized Representative
PT. BLESINDO INDONESIAAR Address
Ruko Duren Sawit Center No. 9B, Jl Duren Sawit Raya
Registration Date
Nov 26, 2020
Expiry Date
Nov 26, 2023
Product Type
Clinical Chemistry Test System
Bilirubin (total and unbound) in the neonate test system (strip & midstream)
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