Taiwan FDA registration c420596e49e561b23e100f4271db3bff
"Pentax" portable bronchoscope
TW: "賓得士" 可攜式支氣管鏡
Taiwan·Risk Class 2·HOYA CORPORATION PENTAX MIYAGI FACTORY·Registered Apr 10, 2006 – Apr 10, 2026ExpiredRegistration details
- Analysis ID
- c420596e49e561b23e100f4271db3bff
- Customs Code
- DHA00601426203
Company information
- Manufacturer
- HOYA CORPORATION PENTAX MIYAGI FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- G ENT Science
- Import Information
- import
Dates and status
- Registration Date
- Apr 10, 2006
- Expiry Date
- Apr 10, 2026
About this record
Access comprehensive regulatory information for "Pentax" portable bronchoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c420596e49e561b23e100f4271db3bff and manufactured by HOYA CORPORATION PENTAX MIYAGI FACTORY. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).
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