BILISOFT 2.0 Phototherapy System - Indonesia BPOM Medical Device Registration
BILISOFT 2.0 Phototherapy System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902911310. The device is manufactured by LUMITEX MEDICAL DEVICES INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GE OPERATIONS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LUMITEX MEDICAL DEVICES INC.Country of Origin
United States
Authorized Representative
PT. GE OPERATIONS INDONESIAAR Address
South Quarter Tower B, Lantai 18-19 Jl. R.A. Kartini, Kav. 8 Kel. Cilandak Barat, Kec. Cilandak Jakarta Selataran 12430
Registration Date
Jul 18, 2023
Expiry Date
May 23, 2028
Product Type
Therapeutic General and Individual Hospital Equipment
Neonatal phototherapy unit.
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