"Pentax" light source and accessories (unsterilized)
Taiwan·Risk Class 1·PENTAX CORPORATION·Registered Apr 10, 2006 – Apr 10, 2011Cancelled- Analysis ID
- 1df2a7bb4878b6f5679f584b1da5a6c7
- Customs Code
- DHA04400352709
- Manufacturer
- PENTAX CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- WHOLE WELL CO., LTD.
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Fiber Optic Light Source and Vehicle (G.4350)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4350 Ear, nose and throat optical fiber light sources and carriers
- Import Information
- import
- Registration Date
- Apr 10, 2006
- Expiry Date
- Apr 10, 2011
- Cancellation Date
- Jul 25, 2014
- Status
- Logged out
- Reason
- 許可證已逾有效期
Top companies providing products similar to ""Pentax" light source and accessories (unsterilized)"
Recently registered similar products
Access comprehensive regulatory information for "Pentax" light source and accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1df2a7bb4878b6f5679f584b1da5a6c7 and manufactured by PENTAX CORPORATION. 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, and 1 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.