Taiwan FDA registration 4f3e7473ede1c7695beb494e9f426c9d
"Pentax" endoscope attachment (unsterilized)
TW: "賓得士" 內視鏡附件(未滅菌)
Taiwan·Risk Class 1·PENTAX TOHOKU CO., LTD.·Registered Apr 24, 2006 – Apr 24, 2011CancelledRegistration details
- Analysis ID
- 4f3e7473ede1c7695beb494e9f426c9d
- Customs Code
- DHA04400417904
Company information
- Manufacturer
- PENTAX TOHOKU CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- WHOLE WELL CO., LTD.
Product details
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Apr 24, 2006
- Expiry Date
- Apr 24, 2011
- Cancellation Date
- Jul 25, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Pentax" endoscope attachment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4f3e7473ede1c7695beb494e9f426c9d and manufactured by PENTAX TOHOKU CO., LTD.. The authorized representative in Taiwan is WHOLE WELL CO., LTD..
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