LABTEST HDL LE - Indonesia BPOM Medical Device Registration
LABTEST HDL LE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101816845. The device is manufactured by LABTEST DIAGNOSTICA S.A. from Brazil, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is WHIRA PITOE JOINT VENTURE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LABTEST DIAGNOSTICA S.A.Country of Origin
Brazil
Authorized Representative
WHIRA PITOE JOINT VENTUREAR Address
RUKO BUARAN PERSADA NO. 10, JL. JEND.POL.SOEKAMTO RT.008/06,KEL.DUREN SAWIT
Registration Date
Nov 26, 2020
Expiry Date
Jan 08, 2025
Product Type
Clinical Chemistry Test System
Lipoprotein test system (kit & cair)
Invitro Diagnostics
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LABTEST Triglycerides Liquiform
LABTEST Cholesterol Liquiform
LABTEST ALT-GPT Liquiform
LABTEST AST-GOT Liquiform
LABTEST CALIBRA H
LABTEST Urea UV
B&E ELECTROLYTE CALIBRATOR
B&E BIO-TECHNOLOGY CO., LTD.
WAP LAB U-50 URINE ANALYZER AND ACCESSORIES
URIT MEDICAL ELECTRONIC CO., LTD.
BIOMAXIMA TOOLS
BIOMAXIMA S.A.
BIOMAXIMA Bilirubin Total DMSO
BIOMAXIMA S.A.
BIOMAXIMA Bilirubin Total
BIOMAXIMA S.A.
BIOMAXIMA Albumin
BIOMAXIMA S.A.
BIOMAXIMA Bilirubin Direct
BIOMAXIMA S.A.
BIOMAXIMA ASAT
BIOMAXIMA S.A
BIOMAXIMA BIONORM
BIOMAXIMA S.A
BIOMAXIMA BIOPATH
BIOMAXIMA S.A.