I-Check Cartridge - BG3 - Indonesia BPOM Medical Device Registration
I-Check Cartridge - BG3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101323451. The device is manufactured by B&E BIO-TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FOSUN DIAGNOSTICS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
B&E BIO-TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. FOSUN DIAGNOSTICS INDONESIAAR Address
FOSUN DIAGNOSTIK INDONESIA
Registration Date
Jul 11, 2023
Expiry Date
Apr 06, 2028
Product Type
Clinical Chemistry Test System
Multi parameter clinical chemistry test system
Invitro Diagnostics
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