AFERsmart Model M 110-230V (AFERsmart Plus™) - Indonesia BPOM Medical Device Registration
AFERsmart Model M 110-230V (AFERsmart Plus™) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805321093. The device is manufactured by MEDICA S.P.A from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FIRST MEDIKACITRA CENTER.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MEDICA S.P.ACountry of Origin
Italy
Authorized Representative
PT. FIRST MEDIKACITRA CENTERAR Address
JL. PASEBAN RAYA NO.21
Registration Date
Dec 30, 2023
Expiry Date
Oct 26, 2027
Product Type
Therapeutic Gastroenterology-Urology Equipment
Blood access device and accessories.
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