CELLAVISION DC-1 and Accessories - Indonesia BPOM Medical Device Registration
CELLAVISION DC-1 and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205026203. The device is manufactured by CELLAVISION AB. from Sweden, 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
CELLAVISION AB.Country of Origin
Sweden
Authorized Representative
PT. SABA INDOMEDIKAAR Address
KOMP.KEDOYA ELOK PLAZA KAV DB/33 KEDOYA SELATAN
Registration Date
Oct 16, 2020
Expiry Date
Aug 17, 2025
Product Type
Automatic and Semi-Automatic Hematology Equipment
Automated cell-locating device.
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