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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.

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BPOM Registered
Risk Class Kelas Resiko : B
SERENITY Neonate LED Phototherapy
Analysis ID: AKL 20902712617

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. SERENITY INDONESIA

AR 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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