Taiwan FDA registration e1f2dc5d7803877290c52b7e99b2fe52
"Taiwan Advanced" Rectal Dilator (Unsterilized)
TW: "台灣先進" 直腸擴張器(未滅菌)
Taiwan·Risk Class 1·TAIWAN SURGICAL CORPORATION·Registered Mar 07, 2014 – Mar 07, 2019CancelledRegistration details
- Analysis ID
- e1f2dc5d7803877290c52b7e99b2fe52
Company information
- Manufacturer
- TAIWAN SURGICAL CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TAIWAN SURGICAL CORPORATION
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
- Domestic
Dates and status
- Registration Date
- Mar 07, 2014
- Expiry Date
- Mar 07, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Taiwan Advanced" 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 e1f2dc5d7803877290c52b7e99b2fe52 and manufactured by TAIWAN SURGICAL CORPORATION. The authorized representative in Taiwan is TAIWAN SURGICAL CORPORATION.
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