SERENITY Neonate LED Phototherapy - Indonesia BPOM Medical Device Registration
SERENITY Neonate LED Phototherapy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902713097. The device is manufactured by ZHENGZHOU DISON INSTRUMENT AND METER CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SERENITY INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ZHENGZHOU DISON INSTRUMENT AND METER CO.,LTD.Country of Origin
China
Authorized Representative
PT. SERENITY INDONESIAAR Address
Komp. Ruko Griya Inti Sentosa Jl. Griya Agung Blok O No. 96 Sunter
Registration Date
Dec 08, 2020
Expiry Date
Aug 25, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Neonatal phototherapy unit.
Non Radiation Electromedics
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