LumiraDx Multi Quality Control - Indonesia BPOM Medical Device Registration
LumiraDx Multi Quality Control is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208420109. The device is manufactured by LUMIRADX UK LTD from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDQUEST GLOBAL PARTNERS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LUMIRADX UK LTDCountry of Origin
United Kingdom
Authorized Representative
PT. MEDQUEST GLOBAL PARTNERSAR Address
MENARA SALEMBA LANTAI 7, JALAN SALEMBA RAYA NOMOR 5-5A
Registration Date
Jun 10, 2024
Expiry Date
Jan 01, 2028
Product Type
Hematological Reagents
Hematology quality control mixture.
Invitro Diagnostics
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NODFORD Anti-Mullerian Hormone/ AMH (CLIA) Kit
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NODFORD Total Triiodothyronine/ TT3 (CLIA) Kit
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NODFORD Free Triiodothyronine/ FT3 (CLIA) Kit
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DIAPRO HSV1 IgM
DIA.PRO DIAGNOSTIC BIOPROBES S.R.L
DIAPRO Chlamydia Trachomatis IgM
DIA.PRO DIAGNOSTIC BIOPROBES S.R.L.
DIAPRO HSV2 IgM
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LumiraDx HbA1c Quality Controls
LUMIRADX UK, LTD.
NODFORD Cardiac troponin I (CLIA) Kit
SHENZHEN NODFORD INDUSTRIAL CO., LTD

