"Pentax" electronic cystoscope
Taiwan·Risk Class 2·HOYA CORPORATION PENTAX MIYAGI FACTORY·Registered Apr 20, 2010 – Apr 20, 2020Cancelled- Analysis ID
- 49a106cd266ff8a40141485642d38013
- Customs Code
- DHA00602091406
- Manufacturer
- HOYA CORPORATION PENTAX MIYAGI FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- WHOLE WELL CO., LTD.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
- Registration Date
- Apr 20, 2010
- Expiry Date
- Apr 20, 2020
- Cancellation Date
- Jun 22, 2022
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Pentax" electronic cystoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 49a106cd266ff8a40141485642d38013 and manufactured by HOYA CORPORATION PENTAX MIYAGI FACTORY. The authorized representative in Taiwan is WHOLE WELL CO., LTD..
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