Pure Global

CONOX Pediatric Sensor - Indonesia BPOM Medical Device Registration

CONOX Pediatric Sensor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21001520004. The device is manufactured by FRESENIUS KABI (NANCHANG) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FRESENIUS KABI 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
CONOX Pediatric Sensor
Analysis ID: AKL 21001520004

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. FRESENIUS KABI INDONESIA

AR Address

Menara Bidakara 1 Lt 19, Jl. Jend Gatot Subroto Kav 71-73

Registration Date

Feb 01, 2025

Expiry Date

Oct 01, 2029

Product Type

Diagnostic Neurology Equipment

Cutaneous electrode.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing