COMBOSTIK™ R-700 and Accessories - Indonesia BPOM Medical Device Registration
COMBOSTIK™ R-700 and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102021048. The device is manufactured by DFI CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SABA INDOMEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DFI CO., LTDCountry of Origin
Korea
Authorized Representative
PT. SABA INDOMEDIKAAR Address
KOMP.KEDOYA ELOK PLAZA KAV DB/33 KEDOYA SELATAN
Registration Date
Feb 25, 2020
Expiry Date
Dec 01, 2024
Product Type
Clinical Laboratory Equipment
Automated urinalysis system.
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