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"C-PRO DIRECT" Limb orthosis (Non-Sterile) - Taiwan Registration 2c5760a57f0330f70e43711e475ebc5c

Access comprehensive regulatory information for "C-PRO DIRECT" Limb orthosis (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 2c5760a57f0330f70e43711e475ebc5c and manufactured by C-Pro Direct Ltd.. The authorized representative in Taiwan is INNOVATIVE HEALTHCARE 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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2c5760a57f0330f70e43711e475ebc5c
Registration Details
Taiwan FDA Registration: 2c5760a57f0330f70e43711e475ebc5c
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Device Details

"C-PRO DIRECT" Limb orthosis (Non-Sterile)
TW: "ๅธŒๆŸๅพท็‘ž็‰น" ่‚ข้ซ”่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2c5760a57f0330f70e43711e475ebc5c

Ministry of Health Medical Device Import No. 016160

DHA09401616005

Company Information

United Kingdom

Product Details

Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.

o Equipment for physical medicine

O3475 Body Equipment

Imported from abroad

Dates and Status

Feb 16, 2016

Feb 16, 2021