Pure Global

Resvent Neonatal Phototherapy Unit - Indonesia BPOM Medical Device Registration

Resvent Neonatal Phototherapy Unit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902025057. The device is manufactured by RESVENT MEDICAL TECHNOLOGY CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SUMBER MAKMUR BERDIKARI.

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
Resvent Neonatal Phototherapy Unit
Analysis ID: AKL 20902025057

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

SUMBER MAKMUR BERDIKARI

AR Address

RUKAN CROWN GREEN LAKE CITY BLOK B NO. 8, PETIR, TANGERANG 15147

Registration Date

Sep 04, 2020

Expiry Date

Jun 11, 2024

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