XENOLITE-NL Series 800 - Indonesia BPOM Medical Device Registration
XENOLITE-NL Series 800 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11503710743. The device is manufactured by LIFE TECH, INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is RAVINDRA PUTRAPRATAMA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
LIFE TECH, INC.Country of Origin
United States
Authorized Representative
RAVINDRA PUTRAPRATAMAAR Address
Pusat Niaga Duta Mas Fatmawati Blok B2-18. Jl. Fatmawati 39 - Cipete Utara Jakarta 12150
Registration Date
May 14, 2020
Expiry Date
Apr 17, 2025
Product Type
Other Radiology Equipment
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