HOSMED Neonatal Incubator Filia - Indonesia BPOM Medical Device Registration
HOSMED Neonatal Incubator Filia is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902125502. The device is manufactured by HOSMED INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SALSABIL RESA PRADANA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HOSMED INC.Country of Origin
United States
Authorized Representative
PT. SALSABIL RESA PRADANAAR Address
Sentral Senayan II Office Tower Lt.16 Unit 216A Jl. Asia Afrika No.6 Jakarta Pusat
Registration Date
Sep 07, 2021
Expiry Date
Apr 16, 2024
Product Type
Therapeutic General and Individual Hospital Equipment
Neonatal incubator.
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