Taiwan FDA registration 657c3fe9be0d4c296f2292fcc7685b20
"Philips" zone catheter
TW: “飛利浦”區克斯導管
Taiwan·Risk Class 2·Philips Image Guided Therapy Corporation·Registered Dec 12, 2005 – Dec 12, 2025ExpiredRegistration details
- Analysis ID
- 657c3fe9be0d4c296f2292fcc7685b20
- Customs Code
- DHA00601379201
Company information
- Manufacturer
- Philips Image Guided Therapy Corporation
- Manufacturer Country
- United States
- Authorized Representative
- LORION ENTERPRISES INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Dec 12, 2005
- Expiry Date
- Dec 12, 2025
About this record
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.
Free DatabasePowered by Pure Global AI89,000+ Devices