"Pentax" electronic upper gastrointestinal endoscope
Taiwan·Risk Class 2·HOYA CORPORATION PENTAX MIYAGI FACTORY·Registered Mar 03, 2010 – Mar 03, 2025Expired- Analysis ID
- ea32437e3771e34be80488364ddfbda3
- Customs Code
- DHA00602062400
- Manufacturer
- HOYA CORPORATION PENTAX MIYAGI FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE)
- 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
- Mar 03, 2010
- Expiry Date
- Mar 03, 2025
Top companies providing products similar to ""Pentax" electronic upper gastrointestinal endoscope"
Recently registered similar products
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 ea32437e3771e34be80488364ddfbda3 and manufactured by HOYA CORPORATION PENTAX MIYAGI FACTORY. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).
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.