iQ Body Fluids Controls-Level I and Level II - Indonesia BPOM Medical Device Registration
iQ Body Fluids Controls-Level I and Level II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208122253. 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 PT. DHH TRADING INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DASH INC.Country of Origin
United States
Authorized Representative
PT. DHH TRADING INDONESIAAR Address
Revenue Tower 19F, Jl. Jenderal Sudirman No. 52-53, Prov. DKI Jakarta, Kota Adm. Jakarta Selatan, Kec Kebayoran Baru, Kel Senayan
Registration Date
Nov 22, 2024
Expiry Date
Mar 28, 2029
Product Type
Hematological Reagents
Hematology quality control mixture.
Invitro Diagnostics
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XN-L CHECK โข L1
WRP Check EX
ADVIA 120/ADVIA 2120/ADVIA 2120i 3in1 TESTpointโข Hematology Controls.
ADVIA 120/ADVIA 2120/ADVIA 2120i 3in1 TESTpoint Hematology Abnormal High Controls
XN CHECKโข L1
EIGHTCHECK - 3WP-N
XN CAL
SYSMEX SCSโข -1000
XN CALโข PF
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