FEROZE LD Lyse - Indonesia BPOM Medical Device Registration
FEROZE LD Lyse is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208320435. 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
Sep 12, 2023
Expiry Date
Feb 11, 2026
Product Type
Hematological Reagents
Red cell lysing reagent.
Invitro Diagnostics
WHEISMAN AC 610 AUTO HEMATOLOGY ANALYZER AND ACCESSORIES
WHEISMAN AC 310 AUTO HEMATOLOGY ANALYZER AND ACCESSORIES
WHEISMAN W-31D Diluent
WHEISMAN W-61LH Lyse
WHEISMAN W-61LD Lyse
WHEISMAN W-61D Diluent
WHEISMAN W-5P Probe Cleanser
FEROZE Diluent
FEROZE Auto 5-part Hematology Analyzer
FEROZE LH Lyse
CHRONALIFEMED IV Catheter Pen Type
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CHRONALIFEMED Non-Absorbable Suture Silk Braided
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CHRONALIFEMED Absorbable Suture Chromic Catgut
SHANDONG HAIDIKE MEDICAL PRODUCTS
CHRONALIFEMED Absorbable Suture Plain Catgut
SHANDONG HAIDIKE MEDICAL PRODUCTS
FEROZE Sheath
URIT MEDICAL ELECTRONIC CO., LTD
FEROZE Reticulocyte Control For Hematology Analyzer
URIT MEDICAL ELECTRONIC CO., LTD
FEROZE Control Material for Hematology Analyzer
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FEROZE Calibrator for Hematology Analyzer
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FEROZE Lyse
URIT MEDICAL ELECTRONIC CO., LTD
FEROZE Diluent 2
URIT MEDICAL ELECTRONIC CO., LTD