Taiwan FDA registration f493f9ec9c85e0f61053213569560b1a
"Uyishi" manual patient transport device
TW: “維醫世”手動病患輸送裝置
Taiwan·Risk Class 1·WYEAST MEDICAL CORPORATION·Registered Mar 11, 2008 – Mar 11, 2013CancelledRegistration details
- Analysis ID
- f493f9ec9c85e0f61053213569560b1a
- Customs Code
- DHA04400656802
Company information
- Manufacturer
- WYEAST MEDICAL CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- Tianqun Medical Enterprise Co., Ltd
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Manual Patient Transport Device (J.6785)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6785 Manual Patient Conveying Device
- Import Information
- import
Dates and status
- Registration Date
- Mar 11, 2008
- Expiry Date
- Mar 11, 2013
- Cancellation Date
- Apr 24, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Uyishi" manual patient transport device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f493f9ec9c85e0f61053213569560b1a and manufactured by WYEAST MEDICAL CORPORATION. The authorized representative in Taiwan is Tianqun Medical Enterprise 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