RIGHTEST Lancing Device GD500 - Indonesia BPOM Medical Device Registration
RIGHTEST Lancing Device GD500 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603421365. The device is manufactured by BIONIME CORPORATION from Taiwan (China), and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. QUALTEK CONSULTANT JAKARTA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
BIONIME CORPORATIONCountry of Origin
Taiwan (China)
Authorized Representative
PT. QUALTEK CONSULTANT JAKARTAAR Address
Icon Business Park Blok K No 6, BSD City, Kab Tangerang, Banten
Registration Date
Jun 25, 2024
Expiry Date
Jan 31, 2029
Product Type
Surgical Equipment
Manual surgical instrument for general use
Non Electromedic Non Sterile
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