BIOMAXIMA BIONORM - Indonesia BPOM Medical Device Registration
BIOMAXIMA BIONORM is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101812265. The device is manufactured by BIOMAXIMA S.A from Poland, 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
BIOMAXIMA S.ACountry of Origin
Poland
Authorized Representative
WHIRA PITOE JOINT VENTUREAR Address
Ruko Buaran Persada NO. 10, Jl. Jend. R.S. Soekanto RT.008 RW.006
Registration Date
Oct 23, 2024
Expiry Date
Aug 08, 2029
Product Type
Clinical Chemistry Test System
Quality control material (assayed and unassayed) (cair)
Invitro Diagnostics
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 ASAT
BIOMAXIMA S.A
BIOMAXIMA Albumin
BIOMAXIMA S.A.
BIOMAXIMA Bilirubin Direct
BIOMAXIMA S.A.
BIOMAXIMA Cholesterol
BIOMAXIMA S.A.
BIOMAXIMA BIOPATH
BIOMAXIMA S.A.