Taiwan FDA registration cb75835b448863fc9eabf9f9172c4d19
"Pentax" ultrasound electronic bronchoscope
TW: “賓得士”超音波電子式支氣管鏡
Taiwan·Risk Class 2·HOYA CORPORATION PENTAX MIYAGI FACTORY·Registered Feb 25, 2010 – Feb 25, 2025ExpiredRegistration details
- Analysis ID
- cb75835b448863fc9eabf9f9172c4d19
- Customs Code
- DHA00602060009
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
- Product Type (Level 2)
- G.4680 Bronchial tubescopes (soft or rigid) and accessories thereof
- Import Information
- import
Dates and status
- Registration Date
- Feb 25, 2010
- Expiry Date
- Feb 25, 2025
About this record
Access comprehensive regulatory information for "Pentax" ultrasound electronic bronchoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cb75835b448863fc9eabf9f9172c4d19 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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