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"CONVULSE" Manual patient transfer device (Non-Sterile) - Taiwan Registration 22889ca90c362a9e248857929ca7635b

Access comprehensive regulatory information for "CONVULSE" Manual patient transfer device (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 22889ca90c362a9e248857929ca7635b and manufactured by CONVULSE CO., LTD. The authorized representative in Taiwan is CONVULSE CO., LTD.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CONVULSE CO., LTD, and 1 recent registrations in the same category. 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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22889ca90c362a9e248857929ca7635b
Registration Details
Taiwan FDA Registration: 22889ca90c362a9e248857929ca7635b
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Device Details

"CONVULSE" Manual patient transfer device (Non-Sterile)
TW: "ๆญฃๆผข"ๆ‰‹ๅ‹•็—…ๆ‚ฃ่ผธ้€่ฃ็ฝฎ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

22889ca90c362a9e248857929ca7635b

Ministry of Health Medical Device Manufacturing Registration No. 008793

Company Information

Taiwan, Province of China

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Manual Patient Transport Device (J.6785)".

J General hospital and personal use equipment

J6785 Manual Patient Conveyor

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2026

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