Taiwan FDA registration 2a6be483ded15f20a273aafd6c25463d
"Ames" Edmant male urethral sling system
TW: “艾梅斯”艾得滿適男性尿道懸吊帶系統
Taiwan·Risk Class 2·AMERICAN MEDICAL SYSTEMS·Registered Feb 23, 2009 – Feb 23, 2014CancelledRegistration details
- Analysis ID
- 2a6be483ded15f20a273aafd6c25463d
- Customs Code
- DHA00601995102
Company information
- Manufacturer
- AMERICAN MEDICAL SYSTEMS
- Manufacturer Country
- United States
- Authorized Representative
- KUANPIRE ENTERPRISES CORPORATION
Product details
- Intended Use
- The AMS Male Urethral Sling System is a mesh sling placed under the urethra to treat stress urinary incontinence in men after prostate surgery.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.3300 Surgical mesh
- Import Information
- import
Dates and status
- Registration Date
- Feb 23, 2009
- Expiry Date
- Feb 23, 2014
- Cancellation Date
- Nov 15, 2016
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Ames" Edmant male urethral sling system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2a6be483ded15f20a273aafd6c25463d and manufactured by AMERICAN MEDICAL SYSTEMS. The authorized representative in Taiwan is KUANPIRE ENTERPRISES CORPORATION.
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