CAPILIA™ TB-Neo Extraction Buffer - Indonesia BPOM Medical Device Registration
CAPILIA™ TB-Neo Extraction Buffer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204914492. The device is manufactured by TAUNS LABORATORIES, INC. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is BRIDGE TWO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
TAUNS LABORATORIES, INC.Country of Origin
Japan
Authorized Representative
BRIDGE TWOAR Address
Petojo Melintang No. 17 Kel. Petojo Selatan, Kec. Gambir Jakarta Pusat
Registration Date
Nov 18, 2021
Expiry Date
Dec 31, 2024
Product Type
Reagents and Specimen Providers
General purpose reagent.
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