Taiwan FDA registration 41c0472314522249264023b515826895
"Covidien" Willie Raiber bipolar electrocautery
TW: "柯惠" 威利雷柏雙極電灼鉗
Registration details
- Analysis ID
- 41c0472314522249264023b515826895
- Customs Code
- DHA00601356006
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)
- I General, Plastic Surgery and Dermatology
- 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" Willie Raiber bipolar electrocautery in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 41c0472314522249264023b515826895 and manufactured by COVIDIEN LLC;; COVID. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.
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