Pure Global

VIDAMED Infant Phototherapy - Indonesia BPOM Medical Device Registration

VIDAMED Infant Phototherapy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902220587. The device is manufactured by SHENZHEN COMEN MEDICAL INSTRUMENT CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ARIMIA JAYA MANDIRI.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
VIDAMED Infant Phototherapy
Analysis ID: AKL 20902220587

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ARIMIA JAYA MANDIRI

AR Address

Gedung Konica lantai 3A Jl. Gunung Sahari Raya nomor 78

Registration Date

Jun 21, 2022

Expiry Date

Jan 01, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Neonatal phototherapy unit.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing