Taiwan FDA registration 46c3a122c54f3118be0778ba719f5d9f
"Pentax" electronic esophageal endoscope
TW: “賓得士”電子式食道內視鏡
Taiwan·Risk Class 2·HOYA CORPORATION PENTAX MIYAGI FACTORY·Registered Apr 03, 2008 – Apr 03, 2028ActiveRegistration details
- Analysis ID
- 46c3a122c54f3118be0778ba719f5d9f
- Customs Code
- DHA00601877602
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)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- import
Dates and status
- Registration Date
- Apr 03, 2008
- Expiry Date
- Apr 03, 2028
About this record
Access comprehensive regulatory information for "Pentax" electronic esophageal endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 46c3a122c54f3118be0778ba719f5d9f 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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