DAY Validation Control - Indonesia BPOM Medical Device Registration
DAY Validation Control is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208129335. The device is manufactured by HAEMOKINESIS LIMITED from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SAKEFA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HAEMOKINESIS LIMITEDCountry of Origin
Switzerland
Authorized Representative
PT. SAKEFAAR Address
Jalan Tarumanegara No.8
Registration Date
Aug 30, 2024
Expiry Date
Jan 08, 2029
Product Type
Hematological Reagents
Hematology quality control mixture.
Invitro Diagnostics
DAY LISS Diluent
DAY Neutral Gel
DAY Anti-B (LB-2)
DAY Anti-D (DVI-) (TH-28)
DAY AHG Gel (Polyspecific anti-human globulin)
STARGEL10 3 Cell Screen
SET DAYcells A1, B
DAY Set Day Cells I-II-III
STARGEL10โข AHG
STATUS1 STAT GROUP CHECK
YINGTAI Low Speed Centrifuge
CHANGSA YINGTAI INSTRUMENT CO.LTD.
YINGTAI DL8M Large Capacity Refrigerated Centrifuge
CHANGSHA YINGTAI INSTRUMENT CO.,LTD
DAY LISS Diluent
HAEMOKINESIS LIMITED
DAY Neutral Gel
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
STARGEL10โข AHG
HAEMOKINESIS LIMITED

