Taiwan FDA registration d727fe2421fb042dd930a69876b0b8ea
Digital color image processor for Pentax endoscopes
TW: "賓得士"內視鏡用數位彩色影像處理器
Taiwan·Risk Class 2·HOYA CORPORATION PENTAX YAMAGATA FACTORY·Registered May 01, 2006 – May 01, 2021CancelledRegistration details
- Analysis ID
- d727fe2421fb042dd930a69876b0b8ea
- Customs Code
- DHA00601437707
Company information
- Manufacturer
- HOYA CORPORATION PENTAX YAMAGATA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- WHOLE WELL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Import Information
- import
Dates and status
- Registration Date
- May 01, 2006
- Expiry Date
- May 01, 2021
- Cancellation Date
- Sep 19, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Digital color image processor for Pentax endoscopes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d727fe2421fb042dd930a69876b0b8ea and manufactured by HOYA CORPORATION PENTAX YAMAGATA FACTORY. The authorized representative in Taiwan is WHOLE WELL CO., LTD..
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