Taiwan FDA registration 6c8cbcbce9888cabab63d62aed09b86b
"Leishi" respiratory rate monitor
TW: “磊仕”呼吸頻率監視器
Taiwan·Risk Class 2·Respironics, Inc.·Registered Jan 16, 2013 – Jan 16, 2023ExpiredRegistration details
- Analysis ID
- 6c8cbcbce9888cabab63d62aed09b86b
- Customs Code
- DHA00602439301
Company information
- Manufacturer
- Respironics, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
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.2375 Respiratory frequency monitor
- Import Information
- import
Dates and status
- Registration Date
- Jan 16, 2013
- Expiry Date
- Jan 16, 2023
About this record
Access comprehensive regulatory information for "Leishi" respiratory rate monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6c8cbcbce9888cabab63d62aed09b86b and manufactured by Respironics, Inc.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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