INTRABEAM 600 - Indonesia BPOM Medical Device Registration
INTRABEAM 600 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21502124271. The device is manufactured by CARL ZEISS MEDITEC AG. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ELO KARSA UTAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CARL ZEISS MEDITEC AG.Country of Origin
Germany
Authorized Representative
PT. ELO KARSA UTAMAAR Address
Jl. Raya Kebayoran Lama No. 34-E, Grogol Selatan, Kebayoran Lama.
Registration Date
Oct 27, 2021
Expiry Date
May 26, 2025
Product Type
Therapeutic Radiology Equipment
X-ray radiation therapy system.
Electromedic Radiation
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