Taiwan FDA registration 9df932e3c5ce63fb3ffd4d187a3adeb5
"Pentax" electronic sigmoid endoscopy
TW: "賓得士" 電子乙狀結腸內視鏡
Taiwan·PENTAX TOHOKU CO., LTD.·Registered Mar 28, 2006 – Mar 28, 2011CancelledRegistration details
- Analysis ID
- 9df932e3c5ce63fb3ffd4d187a3adeb5
- Customs Code
- DHA00601421000
Company information
- Manufacturer
- PENTAX TOHOKU CO., LTD.
- 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
- Mar 28, 2006
- Expiry Date
- Mar 28, 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" electronic sigmoid endoscopy in Taiwan's medical device market through Pure Global AI's free database. is registered under number 9df932e3c5ce63fb3ffd4d187a3adeb5 and manufactured by PENTAX TOHOKU CO., LTD.. The authorized representative in Taiwan is WHOLE WELL CO., LTD..
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