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 20902712617. 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.
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., LTD.Country of Origin
China
Authorized Representative
PT. SERENITY INDONESIAAR Address
Komplek Ruko Permata Kota Blok Q No. 10 Jl. Pangeran Tubagus Angke No.170 RT.010 RW . 01
Registration Date
Jul 24, 2023
Expiry Date
Feb 08, 2028
Product Type
Therapeutic General and Individual Hospital Equipment
Neonatal phototherapy unit.
Non Radiation Electromedics
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