FORA β-Ketone Control Solution Level 1 - Indonesia BPOM Medical Device Registration
FORA β-Ketone Control Solution Level 1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101914469. The device is manufactured by TAIDOC TECHNOLOGY CORPORATION from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INNOVATION HEALTHCARE INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TAIDOC TECHNOLOGY CORPORATIONCountry of Origin
Taiwan (China)
Authorized Representative
PT. INNOVATION HEALTHCARE INDONESIAAR Address
Komplek Ruko Permata Kota, Blok Q No. 11 Jl. Pangeran Tubagus Angke No. 170 Kel. Penjagalan, Kec. Penjaringan, Jakarta Utara 14450
Registration Date
Feb 09, 2023
Expiry Date
Apr 01, 2027
Product Type
Clinical Chemistry Test System
Quality control material (assayed and unassayed) (cair)
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