Taiwan FDA registration de0bb4f8c8366a6918c91d22cb5fbf18
"Pentax" intubated fiber optic endoscope
TW: "賓得士" 插管式光纖內視鏡
Taiwan·PENTAX TOHOKU CO., LTD.·Registered Apr 10, 2006 – Apr 10, 2011CancelledRegistration details
- Analysis ID
- de0bb4f8c8366a6918c91d22cb5fbf18
- Customs Code
- DHA00601426101
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)
- G ENT Science
- Import Information
- import
Dates and status
- Registration Date
- Apr 10, 2006
- Expiry Date
- Apr 10, 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" intubated fiber optic endoscope in Taiwan's medical device market through Pure Global AI's free database. is registered under number de0bb4f8c8366a6918c91d22cb5fbf18 and manufactured by PENTAX TOHOKU CO., LTD.. The authorized representative in Taiwan is WHOLE WELL CO., LTD..
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