"Pentax" electronic nasopharyngeal endoscope
Taiwan·Risk Class 2·HOYA CORPORATION PENTAX MIYAGI FACTORY·Registered Oct 18, 2010 – Oct 18, 2020Cancelled- Analysis ID
- e36918718367fba9c7896cc940d88425
- Customs Code
- DHA00602158100
- 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)
- G ENT Science
- Product Type (Level 2)
- G.4760 Nasopharyngeal scopes (soft or rigid) and their accessories
- Import Information
- import
- Registration Date
- Oct 18, 2010
- Expiry Date
- Oct 18, 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 nasopharyngeal endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e36918718367fba9c7896cc940d88425 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.