"Pentax" light source and accessories (unsterilized)
Taiwan·Risk Class 1·HOYA CORPORATION·Registered Mar 04, 2013 – Mar 04, 2023Expired- Analysis ID
- 5eb86c3cf63e83ae4dde0151292218dc
- Customs Code
- DHA04401276207
- Manufacturer
- HOYA CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE)
- 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
- Mar 04, 2013
- Expiry Date
- Mar 04, 2023
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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 5eb86c3cf63e83ae4dde0151292218dc and manufactured by HOYA CORPORATION. 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 PENTAX 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.