Taiwan FDA registration cfec9ffb8df9a5a51c057b1b23c44525
"Covidien" inflatable and lead-in needle
TW: “柯惠”充氣和導入針
Taiwan·Risk Class 2·COVIDIEN LLC;; Covidien·Registered Aug 14, 2013 – Aug 14, 2028ActiveRegistration details
- Analysis ID
- cfec9ffb8df9a5a51c057b1b23c44525
- Customs Code
- DHA05602537201
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
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Aug 14, 2013
- Expiry Date
- Aug 14, 2028
About this record
Access comprehensive regulatory information for "Covidien" inflatable and lead-in needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cfec9ffb8df9a5a51c057b1b23c44525 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