Taiwan FDA registration 174c334507b05be1c89f76c4bdacbf03
"Le Pulse" vein removal device (sterilized)
TW: “樂脈”靜脈摘除器 (滅菌)
Taiwan·Risk Class 1·LEMAITRE VASCULAR, INC.·Registered Jan 23, 2009 – Jan 23, 2024ExpiredRegistration details
- Analysis ID
- 174c334507b05be1c89f76c4bdacbf03
- Customs Code
- DHA04400742600
Company information
- Manufacturer
- LEMAITRE VASCULAR, INC.
- Manufacturer Country
- United States
- Authorized Representative
- GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH
Product details
- Intended Use
- Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jan 23, 2009
- Expiry Date
- Jan 23, 2024
About this record
Access comprehensive regulatory information for "Le Pulse" vein removal device (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 174c334507b05be1c89f76c4bdacbf03 and manufactured by LEMAITRE VASCULAR, INC.. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.
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