Taiwan FDA registration a577cfa63f39de310fde6d098f567074
"Anwei" pressure regulator (unsterilized)
TW: “安崴”壓力調節器（未滅菌）
Taiwan·Risk Class 1·AMVEX CORPORATION·Registered Jul 13, 2007 – Jul 13, 2012CancelledRegistration details
- Analysis ID
- a577cfa63f39de310fde6d098f567074
- Customs Code
- DHA04400600405
Company information
- Manufacturer
- AMVEX CORPORATION
- Manufacturer Country
- Canada
- Authorized Representative
- CHUNG CHENG MEDICAL EQUIPMENT LTD.
Product details
- Intended Use
- Limited to the first level identification range of the pressure regulator (D.2700) of the management method for medical equipment.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.2700 Pressure Regulator
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jul 13, 2007
- Expiry Date
- Jul 13, 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 "Anwei" pressure regulator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a577cfa63f39de310fde6d098f567074 and manufactured by AMVEX CORPORATION. The authorized representative in Taiwan is CHUNG CHENG MEDICAL EQUIPMENT 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