COMBOSTIK G - Indonesia BPOM Medical Device Registration
COMBOSTIK G is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101010116. The device is manufactured by DFI CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SABA INDOMEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DFI CO., LTD.Country of Origin
Korea
Authorized Representative
SABA INDOMEDIKAAR Address
Ruko Kedoya Elok Plaza DB-33 Jl. Panjang No.7-9
Registration Date
Aug 13, 2024
Expiry Date
Jul 11, 2029
Product Type
Clinical Chemistry Test System
Glucose test system (strip & midstream)
Invitro Diagnostics
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ComboStik 11M (Blood, Bilirubin, Urobilinogen, Ketones, Glucose, Protein, Nitrite, Leukocytes, pH, Specific Gravity, Ascorbic Acid)
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VACUETTE Luer Adapter
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VACUETTE Tube CPDA
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VACUETTE SECONDARY Tube MULTIPLEX PP
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MINICOLLECT Tube CAT Serum Clot Activator
GREINER BIO-ONE GMBH.