Taiwan FDA registration 66b736b42bf1a9134602209ef7998cf5
"Covidien" laparoscopic puncture catheters and adapters
TW: “柯惠” 腹腔鏡穿刺導管及轉接頭
Taiwan·Risk Class 2·COVIDIEN LLC;; COVID·Registered Nov 11, 2005 – Nov 11, 2015CancelledRegistration details
- Analysis ID
- 66b736b42bf1a9134602209ef7998cf5
- Customs Code
- DHA00601355908
Company information
- Manufacturer
- COVIDIEN LLC;; COVID
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Covidien Corporation Limited
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
- Nov 11, 2005
- Expiry Date
- Nov 11, 2015
- Cancellation Date
- Mar 16, 2017
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Covidien" laparoscopic puncture catheters and adapters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 66b736b42bf1a9134602209ef7998cf5 and manufactured by COVIDIEN LLC;; COVID. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.
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