ALPHATOMENDO 300 - Indonesia BPOM Medical Device Registration
ALPHATOMENDO 300 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603514581. The device is manufactured by GIMMI GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SIGMA KARSA MAGNA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GIMMI GMBHCountry of Origin
Germany
Authorized Representative
PT. SIGMA KARSA MAGNAAR Address
Ruko Grosir Cempaka Mas Blok J 38 Jl. Letjend Suprapto
Registration Date
Nov 19, 2019
Expiry Date
May 28, 2024
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
Non Radiation Electromedics
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