Taiwan FDA registration a6a9e7846cd8885061acbd82ce842dda
PengWaves disposable rectal dilator
TW: PengWaves 拋棄式直腸擴張器
Registration details
- Analysis ID
- a6a9e7846cd8885061acbd82ce842dda
- Customs Code
- DHY04300047408
Company information
- Manufacturer
- PENG WAVES ENTERPRISE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PENG WAVES ENTERPRISE CO., LTD.
Product details
- Intended Use
- A device used to dilate the anal dilators and ducts when opening the anus would impede its function, or when an examination instrument is to be inserted.
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5450 Rectal dilator
- Import Information
- Domestic
Dates and status
- Registration Date
- Oct 27, 2005
- Expiry Date
- Oct 27, 2015
- Cancellation Date
- Jun 26, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for PengWaves disposable rectal dilator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a6a9e7846cd8885061acbd82ce842dda and manufactured by PENG WAVES ENTERPRISE CO., LTD.. The authorized representative in Taiwan is PENG WAVES ENTERPRISE CO., LTD..
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