DUOLITH SD1 T-TOP - Indonesia BPOM Medical Device Registration
DUOLITH SD1 T-TOP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403420113. The device is manufactured by STORZ MEDICAL AG from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INNOMED JAYA UTAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
STORZ MEDICAL AGCountry of Origin
Switzerland
Authorized Representative
PT. INNOMED JAYA UTAMAAR Address
Jl. Cideng Barat No.64 #02-01 Kel. Cideng, Kec. Gambir, Jakarta Pusat
Registration Date
Mar 13, 2024
Expiry Date
Dec 31, 2027
Product Type
Therapeutic Physical Health Equipment
Extracorporeal shock wave treatment device
Non Radiation Electromedics
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