Taiwan FDA registration 96178cd64a6dd618bff5cf14bdc8e7d1
Covidien's reusable vascular clamp and remover
TW: “柯惠”可重複使用的血管夾擊發器及移除器
Taiwan·Risk Class 2·COVIDIEN LLC;; Covidien·Registered Nov 17, 2019 – Nov 17, 2029ActiveRegistration details
- Analysis ID
- 96178cd64a6dd618bff5cf14bdc8e7d1
- Customs Code
- DHA05603299706
Company information
- Manufacturer
- COVIDIEN LLC;; Covidien
- Manufacturer Country
- 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
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Nov 17, 2019
- Expiry Date
- Nov 17, 2029
About this record
Access comprehensive regulatory information for Covidien's reusable vascular clamp and remover in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 96178cd64a6dd618bff5cf14bdc8e7d1 and manufactured by COVIDIEN LLC;; Covidien. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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