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"Philips" Trole Coated Balloon Catheter - Taiwan Registration 5efca5e739b409fa5315138ead7a2b16

Access comprehensive regulatory information for "Philips" Trole Coated Balloon Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5efca5e739b409fa5315138ead7a2b16 and manufactured by Philips Image Guided Therapy Corporation. The authorized representative in Taiwan is LORION ENTERPRISES INC..

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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5efca5e739b409fa5315138ead7a2b16
Registration Details
Taiwan FDA Registration: 5efca5e739b409fa5315138ead7a2b16
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Device Details

"Philips" Trole Coated Balloon Catheter
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€ๅธ็‰นๆจ‚ๅก—่—ฅ็ƒๅ›ŠๅฐŽ็ฎก
Risk Class 2

Registration Details

5efca5e739b409fa5315138ead7a2b16

DHA05603380604

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

Jul 02, 2020

Jul 02, 2025