Taiwan FDA registration da493b987053366cf40bcd45c0b108dd
"Pentax" portable fiber optic hysteroscopy
TW: "賓得士"可攜式光纖子宮鏡
Taiwan·Risk Class 2·HOYA CORPORATION PENTAX MIYAGI FACTORY·Registered Apr 06, 2006 – Apr 06, 2021CancelledRegistration details
- Analysis ID
- da493b987053366cf40bcd45c0b108dd
- Customs Code
- DHA00601423806
Company information
- Manufacturer
- HOYA CORPORATION PENTAX MIYAGI FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Import Information
- import
Dates and status
- Registration Date
- Apr 06, 2006
- Expiry Date
- Apr 06, 2021
- Cancellation Date
- Sep 23, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Pentax" portable fiber optic hysteroscopy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number da493b987053366cf40bcd45c0b108dd and manufactured by HOYA CORPORATION PENTAX MIYAGI FACTORY. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).
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