Liquichek Blood Gas Plus E Control Level 3 - Indonesia BPOM Medical Device Registration
Liquichek Blood Gas Plus E Control Level 3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101221659. The device is manufactured by BIORAD LABORATORIES, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DIASTIKA BIOTEKINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIORAD LABORATORIES, INC.Country of Origin
United States
Authorized Representative
PT. DIASTIKA BIOTEKINDOAR Address
Rukan Sentra Pemuda Kav.30 - 31 Jalan Pemuda No.61 RT.009 RW.003 Kel. Rawamangun Kec.Pulogadung
Registration Date
Oct 06, 2022
Expiry Date
May 31, 2025
Product Type
Clinical Chemistry Test System
Quality control material (assayed and unassayed) (cair)
Invitro Diagnostics
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LIQUICHEK Blood Gas Plus E Control Level 1
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LIQUICHEK Blood Gas Plus E Control Level 2
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