Pure Global

KABEMA Ultrasound Diagnostic Systems - Indonesia BPOM Medical Device Registration

KABEMA Ultrasound Diagnostic Systems is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501420230. The device is manufactured by VINNO TECHNOLOGY (SUZHOU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. WORK WITH YOU.

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
KABEMA Ultrasound Diagnostic Systems
Analysis ID: AKL 21501420230

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. WORK WITH YOU

AR Address

KARYA BERSAMA ANDA

Registration Date

Apr 24, 2024

Expiry Date

Dec 31, 2025

Product Type

Diagnostic Radiology Equipment

Ultrasonic pulsed doppler imaging system.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing