Taiwan FDA registration 1a9e6dd79452f034c451c4fcc37ef9ee
"Le Pulse" non-balloon occlusive catheter
TW: “樂脈”非氣球型閉塞導管
Taiwan·Risk Class 2·LEMAITRE VASCULAR, INC.·Registered Nov 20, 2012 – Nov 20, 2017CancelledRegistration details
- Analysis ID
- 1a9e6dd79452f034c451c4fcc37ef9ee
- Customs Code
- DHA00602417208
Company information
- Manufacturer
- LEMAITRE VASCULAR, INC.
- Manufacturer Country
- United States
- Authorized Representative
- GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH
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
- Nov 20, 2012
- Expiry Date
- Nov 20, 2017
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Le Pulse" non-balloon occlusive catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1a9e6dd79452f034c451c4fcc37ef9ee and manufactured by LEMAITRE VASCULAR, INC.. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.
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