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"Philips" zone catheter - Taiwan Registration 657c3fe9be0d4c296f2292fcc7685b20

Access comprehensive regulatory information for "Philips" zone catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 657c3fe9be0d4c296f2292fcc7685b20 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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657c3fe9be0d4c296f2292fcc7685b20
Registration Details
Taiwan FDA Registration: 657c3fe9be0d4c296f2292fcc7685b20
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Device Details

"Philips" zone catheter
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€ๅ€ๅ…‹ๆ–ฏๅฐŽ็ฎก
Risk Class 2

Registration Details

657c3fe9be0d4c296f2292fcc7685b20

DHA00601379201

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

Dec 12, 2005

Dec 12, 2025