Taiwan FDA registration 78b87652b6f031e99fa0d7203733bc73
"Covidien" Curiotracheal intubation
TW: “柯惠”萬靈科食道氣管插管
Taiwan·Risk Class 2·COVIDIEN LLC;; COVID·Registered Aug 18, 2009 – Aug 18, 2019CancelledRegistration details
- Analysis ID
- 78b87652b6f031e99fa0d7203733bc73
- Customs Code
- DHA00602012403
Company information
- Manufacturer
- COVIDIEN LLC;; COVID
- Manufacturer Country
- Mexico;;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)
- D Anesthesiology
- Product Type (Level 2)
- D.5650 Esophageal obstruction
- Import Information
- import
Dates and status
- Registration Date
- Aug 18, 2009
- Expiry Date
- Aug 18, 2019
- Cancellation Date
- Mar 16, 2017
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Covidien" Curiotracheal intubation in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 78b87652b6f031e99fa0d7203733bc73 and manufactured by COVIDIEN LLC;; COVID. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.
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