Taiwan FDA registration 49e6fdbba8194177752524a25ffb7471
“Medtronic” Cardiovascular Surgical Instruments (Non-Sterile)
TW: “美敦力”心臟血管外科器械(未滅菌)
Taiwan·Risk Class 1·MD·Medtronic Inc.·Registered Aug 06, 2013 – Aug 06, 2023ExpiredRegistration details
- Analysis ID
- 49e6fdbba8194177752524a25ffb7471
- License Form
- Ministry of Health Medical Device Import No. 013285
- Customs Code
- DHA09401328500
Company information
- Manufacturer
- Medtronic Inc.
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- Limited to the first level identification range of medical equipment management measures for cardiovascular surgical instruments (E.4500).
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E4500 Cardiovascular Surgical Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 06, 2013
- Expiry Date
- Aug 06, 2023
About this record
Access comprehensive regulatory information for “Medtronic” Cardiovascular Surgical Instruments (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 49e6fdbba8194177752524a25ffb7471 and manufactured by Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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