HUMAN CK MB liquiUV HumaStar - Indonesia BPOM Medical Device Registration
HUMAN CK MB liquiUV HumaStar is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101913368. The device is manufactured by HUMAN GESELLSCHAFT FÜR BIOCHEMICA UND DIAGNOSTICA MBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SALI POLAPA TOGETHER.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Germany
Authorized Representative
PT. SALI POLAPA TOGETHERAR Address
Puri Sentra Niaga Blok B 33-34 Jl. Raya Kalimalang 13620
Registration Date
Feb 23, 2023
Expiry Date
Dec 31, 2027
Product Type
Clinical Chemistry Test System
Creatine phosphokinase/creatine kinase or isoenzymes test system(kit & cair)
Invitro Diagnostics
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HUMAN SODIUM LIQUICOLOR
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HUMAN Cystatin-C Liquidirect Controls
HUMAN Calcium Liquicolor HumaStar
HUMAN Transferrin
HUMAN MICROALBUMIN
HUMAN CK NAC LiquiUV HumaStar
HUMAN HumaSRate 24PT and Accessories
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HUMAN CRP Control HumaFIA SR
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HUMAN IL-6 HumaFIA SR
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HUMAN D-Dimer HumaFIA SR
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HUMAN SLE LATEX TEST
HUMAN GESELLSCHAFT FÜR BIOCHEMICA UND DIAGNOSTICA MBH
HUMAN Creatinine (enzym) Liquicolor HumaStar
HUMAN GESELLSCHAFT FÜR BIOCHEMICA UND DIAGNOSTICA MBH
HUMAN SODIUM LIQUICOLOR
HUMAN GESELLSCHAFT FÜR BIOCHEMICA UND DIAGNOSTICA MBH
HUMAN Transferrin
HUMAN GESELLSCHAFT FÜR BIOCHEMICA UND DIAGNOSTICA MBH