Amnotom 160 Base - Indonesia BPOM Medical Device Registration
Amnotom 160 Base is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603421130. The device is manufactured by ALSA APPARECCHI MEDICALI S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is DUA SRIKANDI INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ALSA APPARECCHI MEDICALI S.R.L.Country of Origin
Italy
Authorized Representative
DUA SRIKANDI INDONESIAAR Address
DUA SRIKANDI INDONESIA
Registration Date
May 29, 2024
Expiry Date
Dec 31, 2026
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
Non Radiation Electromedics
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