DUOLITH SD1 Tower - Indonesia BPOM Medical Device Registration
DUOLITH SD1 Tower is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31403320497. The device is manufactured by STORZ MEDICAL AG from Switzerland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is INNOMED JAYA UTAMA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
STORZ MEDICAL AGCountry of Origin
Switzerland
Authorized Representative
INNOMED JAYA UTAMAAR Address
Jl. Cideng Barat No.64 #02-01, Cideng Barat nomor 64 #02-01, Kel. Cideng, Kec. Gambir, Jakarta Pusat, DKI Jakarta
Registration Date
Apr 04, 2023
Expiry Date
Dec 31, 2023
Product Type
Therapeutic Physical Health Equipment
Extracorporeal Shock Wave Treatment
Non Radiation Electromedics
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