Taiwan FDA registration 25d0ba5eccca7986a80ab8f5fe1b10df
"Philips" Zone Extreme/Select Support Catheter
TW: “飛利浦”區克斯極緻/選擇支撐導管
Taiwan·Risk Class 2·Philips Image Guided Therapy Corporation·Registered Jun 14, 2013 – Jun 14, 2028ActiveRegistration details
- Analysis ID
- 25d0ba5eccca7986a80ab8f5fe1b10df
- Customs Code
- DHA00602497405
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
- Jun 14, 2013
- Expiry Date
- Jun 14, 2028
About this record
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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