SuperFlex D-Dimer Kit - Indonesia BPOM Medical Device Registration
SuperFlex D-Dimer Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207420135. The device is manufactured by SUZHOU SYM-BIO LIFESCIENCE CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is DARMA LABORA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SUZHOU SYM-BIO LIFESCIENCE CO., LTDCountry of Origin
China
Authorized Representative
DARMA LABORA INDONESIAAR Address
KAWASAN INDUSTRI JABABEKA 7, BLOK B3/B, DESA WANGUNHARJA
Registration Date
Aug 28, 2024
Expiry Date
Apr 24, 2029
Product Type
Haematology Package and Kit
Fibrinogen/fibrin degradation products assay.
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SuperFlex Automated Chemiluminescence Analyzer
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SuperFlex Serum Amyloid A Kit
SUZHOU SYM-BIO LIFESCIENCE CO., LTD
SuperFlex All in One C-Reactive Protein Kit
SUZHOU SYM-BIO LIFESCIENCE CO., LTD
SuperFlex IL-6 Control
SUZHOU SYM-BIO LIFESCIENCE CO., LTD
SuperFlex SAA Control
SUZHOU SYM-BIO LIFESCIENCE CO., LTD
SuperFlex MYO Control
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SuperFlex CRP Control
SUZHOU SYM-BIO LIFESCIENCE CO., LTD.
SuperFlex NT-proBNP Control
SUZHOU SYM-BIO LIFESCIENCE CO., LTD