Taiwan FDA registration ec2380835a2786a0b5f21e83c01a1d66
"Mattens" pain-relieving gas supply
TW: "瑪特司"止痛氣體供應機
Taiwan·Risk Class 2·MATRX BY MIDMARK·Registered Jan 22, 2007 – Jan 22, 2012CancelledRegistration details
- Analysis ID
- ec2380835a2786a0b5f21e83c01a1d66
- Customs Code
- DHA00601771006
Company information
- Manufacturer
- MATRX BY MIDMARK
- Manufacturer Country
- United States
- Authorized Representative
- YI LIN ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, please refer to the approved version of Chinese copy
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5160 Anesthesia or analgesic gas supply machine
- Import Information
- import
Dates and status
- Registration Date
- Jan 22, 2007
- Expiry Date
- Jan 22, 2012
- Cancellation Date
- Apr 30, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Mattens" pain-relieving gas supply in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ec2380835a2786a0b5f21e83c01a1d66 and manufactured by MATRX BY MIDMARK. The authorized representative in Taiwan is YI LIN 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