Taiwan FDA registration db842529e7939126a1d4957771dd1b23
"Le Pulse" Retis thrombus removal catheter
TW: “樂脈”雷緹斯血栓清除導管
Taiwan·Risk Class 2·LEMAITRE VASCULAR, INC.·Registered May 16, 2011 – May 16, 2026ExpiredRegistration details
- Analysis ID
- db842529e7939126a1d4957771dd1b23
- Customs Code
- DHA00602231303
Company information
- Manufacturer
- LEMAITRE VASCULAR, INC.
- Manufacturer Country
- United States
- Authorized Representative
- HSIN TUNG MEDICAL CO., LTD.
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.5150 血栓切除術導管
- Import Information
- import
Dates and status
- Registration Date
- May 16, 2011
- Expiry Date
- May 16, 2026
About this record
Access comprehensive regulatory information for "Le Pulse" Retis thrombus removal catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number db842529e7939126a1d4957771dd1b23 and manufactured by LEMAITRE VASCULAR, INC.. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..
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