Pure Global

YINGCHI Pulsed Magnetic Stimulation Device - Indonesia BPOM Medical Device Registration

YINGCHI Pulsed Magnetic Stimulation Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003420083. The device is manufactured by SHENZHEN YINGCHI TECHNOLOGY CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PANAMED ANUGERAH ABADI.

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
YINGCHI Pulsed Magnetic Stimulation Device
Analysis ID: AKL 21003420083

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. PANAMED ANUGERAH ABADI

AR Address

APL Tower 6th Floor Suite 3 Jalan Letjen S. Parman Kavling 28

Registration Date

Aug 21, 2024

Expiry Date

May 28, 2027

Product Type

Therapeutic Neurology Equipment

Repetitive transcranial magnetic stimulation system

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from SHENZHEN YINGCHI TECHNOLOGY CO.,LTD.
Products from the same manufacturer (1 products)