FEROZE Diluent - Indonesia BPOM Medical Device Registration
FEROZE Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208320501. The device is manufactured by WHEISMAN MEDICAL TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BUANA INTIPRIMA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
WHEISMAN MEDICAL TECHNOLOGY CO., LTDCountry of Origin
China
Authorized Representative
PT. BUANA INTIPRIMA MEDIKAAR Address
Rukan Sentra Niaga Green Lake City Blok F No.3
Registration Date
Oct 27, 2023
Expiry Date
Mar 24, 2026
Product Type
Hematological Reagents
Blood cell diluents
Invitro Diagnostics
WHEISMAN AC 610 AUTO HEMATOLOGY ANALYZER AND ACCESSORIES
WHEISMAN AC 310 AUTO HEMATOLOGY ANALYZER AND ACCESSORIES
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WHEISMAN W-31D Diluent
WHEISMAN W-5P Probe Cleanser
WHEISMAN W-61D Diluent
FEROZE Auto 5-part Hematology Analyzer
FEROZE LH Lyse
FEROZE Probe Cleanser
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CHRONALIFEMED Absorbable Suture Chromic Catgut
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CHRONALIFEMED Absorbable Suture Plain Catgut
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FEROZE Sheath
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FEROZE Reticulocyte Control For Hematology Analyzer
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FEROZE Control Material for Hematology Analyzer
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FEROZE Calibrator for Hematology Analyzer
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FEROZE Lyse
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FEROZE Diluent 2
URIT MEDICAL ELECTRONIC CO., LTD