Taiwan FDA registration 49af86043b2ffdddb7dd2f71a8174c94
Reid endotracheal tube maintainer (unsterilized)
TW: 雷德氣管內管維持器(未滅菌)
Taiwan·Risk Class 1·LAERDAL MEDICAL AS·Registered Apr 15, 2006 – Apr 15, 2016CancelledRegistration details
- Analysis ID
- 49af86043b2ffdddb7dd2f71a8174c94
- Customs Code
- DHA04400393103
Company information
- Manufacturer
- LAERDAL MEDICAL AS
- Manufacturer Country
- Norway
- Authorized Representative
- Xinyi Co., Ltd
Product details
- Intended Use
- Limited to the first level recognition range of breathing tube support (D.5280) of the medical device management method.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5280 呼吸管路支撐物
- Import Information
- import
Dates and status
- Registration Date
- Apr 15, 2006
- Expiry Date
- Apr 15, 2016
- Cancellation Date
- Aug 09, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Reid endotracheal tube maintainer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 49af86043b2ffdddb7dd2f71a8174c94 and manufactured by LAERDAL MEDICAL AS. The authorized representative in Taiwan is Xinyi Co., 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