Pure Global

"Covidien" Kentley compression sleeve - Taiwan Registration b5dc4140f8c71b59effebed8d0831952

Access comprehensive regulatory information for "Covidien" Kentley compression sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b5dc4140f8c71b59effebed8d0831952 and manufactured by COVIDIEN LLC;; COVID. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.

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
b5dc4140f8c71b59effebed8d0831952
Registration Details
Taiwan FDA Registration: b5dc4140f8c71b59effebed8d0831952
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Covidien" Kentley compression sleeve
TW: โ€œๆŸฏๆƒ โ€่‚ฏ็‰นๅˆฉๅฃ“็ธฎๅฅ—
Risk Class 2
Cancelled

Registration Details

b5dc4140f8c71b59effebed8d0831952

DHA00602438502

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.5800 Compression sleeves for limbs

import

Dates and Status

Jan 07, 2013

Jan 07, 2018

Mar 16, 2017

Cancellation Information

Logged out

ๅ…ฌๅธๆญ‡ๆฅญ