ELEKTA Active Breathing Coordinator - Indonesia BPOM Medical Device Registration
ELEKTA Active Breathing Coordinator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21502320104. The device is manufactured by AKTINA MEDICAL CORPORATION from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ELEKTA MEDICAL SOLUTIONS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AKTINA MEDICAL CORPORATIONCountry of Origin
United States
Authorized Representative
PT. ELEKTA MEDICAL SOLUTIONSAR Address
Cowell Tower Lantai 7 Unit 02A, Jl. Senen Raya No. 135, Kode Pos 10410, Kel. Senen, Kec. Senen, Kota Jakarta Pusat, Prov. DKI Jakarta
Registration Date
Aug 09, 2023
Expiry Date
Aug 01, 2027
Product Type
Therapeutic Radiology Equipment
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