TMS 30i Automated Clinical Analyzer and Accesories - Indonesia BPOM Medical Device Registration
TMS 30i Automated Clinical Analyzer and Accesories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102025269. The device is manufactured by FANDF CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SUMBERMITRA AGUNGJAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FANDF CO., LTD.Country of Origin
Japan
Authorized Representative
PT. SUMBERMITRA AGUNGJAYAAR Address
Gading Bukit Indah, Blok H/3 Kel Kelapa Gading Barat, Kec Kelapa Gading Jakarta Utara
Registration Date
Nov 19, 2024
Expiry Date
Oct 15, 2029
Product Type
Clinical Laboratory Equipment
Instrumentation for clinical multiplex test systems.
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