GEKO ™ T-3 - Indonesia BPOM Medical Device Registration
GEKO ™ T-3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403320420. The device is manufactured by FIRSTKIND LIMITED from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is CEKINDO BUSINESS INTERNATIONAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FIRSTKIND LIMITEDCountry of Origin
United Kingdom
Authorized Representative
CEKINDO BUSINESS INTERNATIONALAR Address
CEKINDO BUSINESS INTERNATIONAL
Registration Date
Jan 26, 2023
Expiry Date
Oct 18, 2027
Product Type
Therapeutic Physical Health Equipment
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