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 20902712619. 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 SERENITY INDONESIA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
ZHENGZHOU DISON INSTRUMENT AND METER CO.,LTDCountry of Origin
China
Authorized Representative
SERENITY INDONESIAAR Address
Komp. Ruko Griya Inti Sentosa Jl. Griya Agung Blok O No. 96 Sunter
Registration Date
Dec 15, 2020
Expiry Date
Aug 25, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Neonatal phototherapy unit.
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