CLINIQA Liquid QC® Cardiac Marker Control VS - Indonesia BPOM Medical Device Registration
CLINIQA Liquid QC® Cardiac Marker Control VS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101024403. The device is manufactured by CLINIQA CORPORATION from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is EMERALINDO ASIA PACIFIC.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CLINIQA CORPORATIONCountry of Origin
United States
Authorized Representative
EMERALINDO ASIA PACIFICAR Address
RUKAN PERMATA SENAYAN BLOK G15, Lantai 1, JL.TENTARA PELAJAR NO. 5, Desa/Kelurahan Grogol Utara, Kec. Kebayoran Lama, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta Kode Pos: 12210
Registration Date
Feb 01, 2024
Expiry Date
Feb 24, 2028
Product Type
Clinical Chemistry Test System
Quality control material (assayed and unassayed) (cair)
Invitro Diagnostics
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i-STAT CK-MB Control Level 1
I-STAT CK-MB Control Level 3
i-STAT CK-MB Control Level 2
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