Platelet Check L1 - Indonesia BPOM Medical Device Registration
Platelet Check L1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208420223. The device is manufactured by DASH INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is Sysmex Indonesia.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DASH INC.Country of Origin
United States
Authorized Representative
Sysmex IndonesiaAR Address
Cyber 2 Tower, 5th Floor Unit E Jl. HR. Rasuna Said Blok X.5 No.13
Registration Date
Aug 26, 2024
Expiry Date
Jan 16, 2028
Product Type
Hematological Reagents
Hematology quality control mixture.
Invitro Diagnostics
iQ Body Fluids Controls-Level I and Level II
XN-L CHECK ™ L1
WRP Check EX
ADVIA 120/ADVIA 2120/ADVIA 2120i 3in1 TESTpoint™ Hematology Controls.
ADVIA 120/ADVIA 2120/ADVIA 2120i 3in1 TESTpoint Hematology Abnormal High Controls
XN CHECK™ L1
EIGHTCHECK - 3WP-N
XN CAL
SYSMEX SCS™ -1000
XN CAL™ PF
EIGHTCHECK-3WP-L
DASH, INC.
XN CHECK L1
DASH, INC.
EIGHTCHECK-3WP-H
DASH, INC.
XN CHECK BF L2
DASH, INC.
XN-L CHECK L2
DASH, INC.
XN CHECK BF L1
DASH, INC.
XN CHECK L3
DASH, INC.
XN CAL
DASH, INC.
XN-L CHECK L3
DASH, INC.
XN CHECK L2
DASH, INC.