Taiwan FDA registration be52fc2b45cdf0af1af171c4af9be233
"Covidien" puncture sleeve double diameter head
TW: “柯惠” 穿刺套管雙徑頭
Taiwan·Risk Class 2·COVIDIEN LLC;; Covidien·Registered Jun 29, 2005 – Jun 29, 2020CancelledRegistration details
- Analysis ID
- be52fc2b45cdf0af1af171c4af9be233
- Customs Code
- DHA00601149205
Company information
- Manufacturer
- COVIDIEN LLC;; Covidien
- Manufacturer Country
- Dominican Republic;;United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Import Information
- import
Dates and status
- Registration Date
- Jun 29, 2005
- Expiry Date
- Jun 29, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Covidien" puncture sleeve double diameter head in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number be52fc2b45cdf0af1af171c4af9be233 and manufactured by COVIDIEN LLC;; Covidien. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices