Taiwan FDA registration c0ad40086e2f8b8891abb55a4c6376ed
"Atrium" vascular tunneler (sterilization)
TW: “心房”血管隧道器 (滅菌)
Taiwan·Risk Class 1·ATRIUM MEDICAL CORPORATION·Registered Jan 15, 2007 – Jan 15, 2012CancelledRegistration details
- Analysis ID
- c0ad40086e2f8b8891abb55a4c6376ed
- Customs Code
- DHA04400552808
Company information
- Manufacturer
- ATRIUM MEDICAL CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- Huangfa Co., Ltd
Product details
- Intended Use
- Limited to the first level identification range of medical equipment management measures for cardiovascular surgical instruments (E.4500).
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.4500 心臟血管外科器械
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jan 15, 2007
- Expiry Date
- Jan 15, 2012
- Cancellation Date
- May 05, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Atrium" vascular tunneler (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c0ad40086e2f8b8891abb55a4c6376ed and manufactured by ATRIUM MEDICAL CORPORATION. The authorized representative in Taiwan is Huangfa Co., Ltd.
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