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"Philips" Zone Extreme/Select Support Catheter - Taiwan Registration 25d0ba5eccca7986a80ab8f5fe1b10df

Access comprehensive regulatory information for "Philips" Zone Extreme/Select Support Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 25d0ba5eccca7986a80ab8f5fe1b10df and manufactured by Philips Image Guided Therapy Corporation. The authorized representative in Taiwan is LORION ENTERPRISES INC..

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25d0ba5eccca7986a80ab8f5fe1b10df
Registration Details
Taiwan FDA Registration: 25d0ba5eccca7986a80ab8f5fe1b10df
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Device Details

"Philips" Zone Extreme/Select Support Catheter
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€ๅ€ๅ…‹ๆ–ฏๆฅต็ทป/้ธๆ“‡ๆ”ฏๆ’ๅฐŽ็ฎก
Risk Class 2

Registration Details

25d0ba5eccca7986a80ab8f5fe1b10df

DHA00602497405

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.1250 Percutaneous catheters

import

Dates and Status

Jun 14, 2013

Jun 14, 2028