Taiwan FDA registration 2c0ff1316462baf3f5852ed50849d682
"Bishi" Patient Exit Monitor (Unsterilized)
TW: “比思希” 病患離床監視器 (未滅菌)
Taiwan·Risk Class 1·PERSONAL SAFETY CORPORATION·Registered Oct 30, 2009 – Oct 30, 2014CancelledRegistration details
- Analysis ID
- 2c0ff1316462baf3f5852ed50849d682
- Customs Code
- DHA04400826007
Company information
- Manufacturer
- PERSONAL SAFETY CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- Tianqun Medical Enterprise Co., Ltd
Product details
- Intended Use
- Limited to the first level recognition range of the Bedside Patient Monitor (J.2400) of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.2400 Bedside Patient Monitor
- Import Information
- import
Dates and status
- Registration Date
- Oct 30, 2009
- Expiry Date
- Oct 30, 2014
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bishi" Patient Exit Monitor (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2c0ff1316462baf3f5852ed50849d682 and manufactured by PERSONAL SAFETY 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