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"Meiqiang" ultrasound therapy device - Taiwan Registration b7a3fd204641bb1ae2ec33f98198e061

Access comprehensive regulatory information for "Meiqiang" ultrasound therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b7a3fd204641bb1ae2ec33f98198e061 and manufactured by METRON MEDICAL AUSTRALIA PTY LTD.. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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b7a3fd204641bb1ae2ec33f98198e061
Registration Details
Taiwan FDA Registration: b7a3fd204641bb1ae2ec33f98198e061
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Device Details

"Meiqiang" ultrasound therapy device
TW: "็พŽๅผท" ่ถ…้Ÿณๆณขๆฒป็™‚ๅ™จ
Risk Class 2
Cancelled

Registration Details

b7a3fd204641bb1ae2ec33f98198e061

DHA00601124208

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

o Physical Medical Sciences

import

Dates and Status

May 02, 2005

May 02, 2020

May 19, 2022

Cancellation Information

Logged out

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