Taiwan FDA registration 037254699c3dd1fd7d565b024b394ab2
"Meride" rectal dilator (unsterilized)
TW: "美瑞德" 直腸擴張器 (未滅菌)
Taiwan·Risk Class 1·MEDRAD, INC.·Registered Apr 24, 2013 – Apr 24, 2018CancelledRegistration details
- Analysis ID
- 037254699c3dd1fd7d565b024b394ab2
- Customs Code
- DHA04401293601
Company information
- Manufacturer
- MEDRAD, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Qiatai Enterprise Co., Ltd
Product details
- Intended Use
- Limited to the first level identification range of "rectal dilator (H.5450)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5450 Rectal dilator
- Import Information
- import
Dates and status
- Registration Date
- Apr 24, 2013
- Expiry Date
- Apr 24, 2018
- Cancellation Date
- Nov 15, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Meride" rectal dilator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 037254699c3dd1fd7d565b024b394ab2 and manufactured by MEDRAD, INC.. The authorized representative in Taiwan is Qiatai Enterprise Co., Ltd.
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