Pure Global

“ME”Back Suppor t(Non-sterile) - Taiwan Registration da5412861d2cec103038f41fa57cf391

Access comprehensive regulatory information for “ME”Back Suppor t(Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number da5412861d2cec103038f41fa57cf391 and manufactured by Mingyi Disability Rehabilitation Equipment Co., Ltd. The authorized representative in Taiwan is Mingyi Disability Rehabilitation Equipment 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
da5412861d2cec103038f41fa57cf391
Registration Details
Taiwan FDA Registration: da5412861d2cec103038f41fa57cf391
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“ME”Back Suppor t(Non-sterile)
TW: “明憶”軟背架 (未滅菌)
Risk Class 1
MD

Registration Details

da5412861d2cec103038f41fa57cf391

Ministry of Health Medical Device Manufacturing Registration No. 001327

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Torso Equipment (O.3490)".

o Equipment for physical medicine

O3490 Torso Gear

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2026