Taiwan FDA registration cc42bdf87bb557de81224e7fa57edc57
"Medi" Ruibang hernia repair net
TW: “美迪”瑞邦疝氣修補網
Taiwan·Risk Class 2·MINNESOTA MEDICAL DEVELOPMENT, INC.·Registered Mar 17, 2011 – Mar 17, 2016CancelledRegistration details
- Analysis ID
- cc42bdf87bb557de81224e7fa57edc57
- Customs Code
- DHA00602213008
Company information
- Manufacturer
- MINNESOTA MEDICAL DEVELOPMENT, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Chengyi Limited
Product details
- Intended Use
- This product is used to assist in hernia repair and reinforcement or other soft tissue defects that can be supported with non-absorbable materials.
- 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
- Mar 17, 2011
- Expiry Date
- Mar 17, 2016
- Cancellation Date
- Aug 13, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Medi" Ruibang hernia repair net in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cc42bdf87bb557de81224e7fa57edc57 and manufactured by MINNESOTA MEDICAL DEVELOPMENT, INC.. The authorized representative in Taiwan is Chengyi Limited.
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