Taiwan FDA registration 5efca5e739b409fa5315138ead7a2b16
"Philips" Trole Coated Balloon Catheter
TW: “飛利浦”司特樂塗藥球囊導管
Taiwan·Risk Class 2·Philips Image Guided Therapy Corporation·Registered Jul 02, 2020 – Jul 02, 2025ExpiredRegistration details
- Analysis ID
- 5efca5e739b409fa5315138ead7a2b16
- Customs Code
- DHA05603380604
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
- Jul 02, 2020
- Expiry Date
- Jul 02, 2025
About this record
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..
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