HUMAN Hemostat Control Plasma Abnormal - Indonesia BPOM Medical Device Registration
HUMAN Hemostat Control Plasma Abnormal is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208023601. 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
Sep 17, 2024
Expiry Date
Nov 08, 2027
Product Type
Hematological Reagents
Hematology quality control mixture.
Invitro Diagnostics
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HUMAN Ca Filling Solution HumaLyte Plus
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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
SHENZHEN YHLO BIOTECH CO., LTD.
HUMAN Ferritin Control HumaFIA SR
BEIJING HUMADX TECH CO., LTD.
HUMAN NT-proBNP Control HumaFIA SR
BEIJING HUMADX TECH CO., LTD.
HUMAN CRP Control HumaFIA SR
BEIJING HUMADX TECH CO., LTD.
HUMAN IL-6 HumaFIA SR
BEIJING HUMADX TECH CO., LTD.
HUMAN D-Dimer HumaFIA SR
BEIJING HUMADX TECH CO., LTD.
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