"Pentax" electronic upper gastrointestinal endoscope
Taiwan·Risk Class 2·HOYA CORPORATION PENTAX MIYAGI FACTORY·Registered Mar 14, 2006 – Mar 14, 2016Cancelled- Analysis ID
- 02c2c35b209aa8455bb4e72eeddefc91
- Customs Code
- DHA00601412700
- 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
- Import Information
- import
- Registration Date
- Mar 14, 2006
- Expiry Date
- Mar 14, 2016
- Cancellation Date
- May 28, 2018
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Pentax" electronic upper gastrointestinal endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 02c2c35b209aa8455bb4e72eeddefc91 and manufactured by HOYA CORPORATION PENTAX MIYAGI FACTORY. The authorized representative in Taiwan is WHOLE WELL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HOYA CORPORATION PENTAX MIYAGI FACTORY, and 2 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.