Taiwan FDA registration 50e09b9d94d21d582c7eb5ecf0fcb36b
"Medtronic" laser shield endotracheal tube
TW: “美敦力”雷射盾氣管內管
Taiwan·Risk Class 2·MEDTRONIC XOMED, INC.·Registered Nov 17, 2010 – Nov 17, 2020CancelledRegistration details
- Analysis ID
- 50e09b9d94d21d582c7eb5ecf0fcb36b
- Customs Code
- DHA00602170808
Company information
- Manufacturer
- MEDTRONIC XOMED, INC.
- Manufacturer Country
- 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)
- D Anesthesiology
- Product Type (Level 2)
- D.5730 Endotracheal tubes
- Import Information
- import
Dates and status
- Registration Date
- Nov 17, 2010
- Expiry Date
- Nov 17, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Medtronic" laser shield endotracheal tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 50e09b9d94d21d582c7eb5ecf0fcb36b and manufactured by MEDTRONIC XOMED, INC.. 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