YINGTAI Low Speed Centrifuge - Indonesia BPOM Medical Device Registration
YINGTAI Low Speed Centrifuge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209122141. The device is manufactured by CHANGSA YINGTAI INSTRUMENT CO.LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SAKEFA.
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 : 2
Manufacturer
CHANGSA YINGTAI INSTRUMENT CO.LTD.Country of Origin
China
Authorized Representative
PT. SAKEFAAR Address
Jalan Tarumanegara No.8
Registration Date
Dec 16, 2024
Expiry Date
Jan 26, 2027
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Automated cell-washing centrifuge for immuno-hematology.
Invitro Diagnostics
YINGTAI DL8M Large Capacity Refrigerated Centrifuge
CHANGSHA YINGTAI INSTRUMENT CO.,LTD
DAY LISS Diluent
HAEMOKINESIS LIMITED
DAY Neutral Gel
HAEMOKINESIS LIMITED
DAY Validation Control
HAEMOKINESIS LIMITED
DAY Anti-B (LB-2)
HAEMOKINESIS LIMITED
DAY Anti-D (DVI-) (TH-28)
HAEMOKINESIS LIMITED
STARGEL10 3 Cell Screen
HAEMOKINESIS LIMITED
SET DAYcells A1, B
HAEMOKINESIS LIMITED
DAY Set Day Cells I-II-III
HAEMOKINESIS LIMITED
STARGEL10™ AHG
HAEMOKINESIS LIMITED