WANTAI Anti-HCV ELISA Kit - Indonesia BPOM Medical Device Registration
WANTAI Anti-HCV ELISA Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30305810555. The device is manufactured by BEIJING WANTAI BIOLOGICAL PHARMACY ENTERPRISE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. SUMIFIN CITRA ABADI.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 3
Country of Origin
China
Authorized Representative
PT. SUMIFIN CITRA ABADIAR Address
Ruko Banjar Wijaya Blok B1 No. 7 Kel. Poris Plawad Indah, Kec. Cipondoh, Tangerang, Banten
Registration Date
Aug 12, 2021
Expiry Date
Jun 28, 2026
Product Type
Immunological Test System
Antinuclear antibody immunological test system.
Invitro Diagnostics
DIAFIN DFRC-24A Refrigerated Centrifuge
CHANGSHA YINGTAI INSTRUMENT CO. LTD.,
DIAFIN DFLC-22 Low Speed Centrifuge
CHANGSHA YINGTAI INSTRUMENT CO. LTD.,
DIAFIN DFLC-30 Clinical Centrifuge
CHANGSHA YINGTAI INSTRUMENT CO. LTD.,
ZENIX Glycated Hemoglobin Test kit (HPLC)
SHENZHEN XILAIHENG MEDICAL ELECTRONICS CO., LTD.
DIAFIN DFRC-12A Refrigerated Centrifuge
CHANGSHA YINGTAI INSTRUMENT CO. LTD.,
DIAFIN DFRC-12B Refrigerated Centrifuge and Accessories
CHANGSHA YINGTAI INSTRUMENT CO. LTD.,
INNODX TSH CMIA
XIAMEN INNODX BIOTECH CO., LTD.
ZELL-ESR Erythrocyte Sedimentation Rate Analyzer
STERILE SAFEQUIP AND CHEMICALS LLP
KEWEI RV-IgM Test Kit
BEIJING KEWEI CLINICAL DIAGNOSTIC REAGENT INC
DIAFIN DFGC-23 Blood Gel Cards Centrifuge
CHANGSHA YINGTAI INSTRUMENT CO. LTD.,

