GAREA Transcutaneous Jaundice Detector - Indonesia BPOM Medical Device Registration
GAREA Transcutaneous Jaundice Detector is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101421145. The device is manufactured by SHENZHEN LUCKCOME TECHNOLOGY INC., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. UBC MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENZHEN LUCKCOME TECHNOLOGY INC., LTD.Country of Origin
China
Authorized Representative
PT. UBC MEDICAL INDONESIAAR Address
Jalan Rawa Gelam V, Blok L Kav. 11-13, Kawasan Industri Pulogadung Jakarta Timur13930
Registration Date
Jun 12, 2024
Expiry Date
Sep 30, 2026
Product Type
Clinical Chemistry Test System
Bilirubin (total and unbound) in the neonate test system
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