Taiwan FDA registration bfeb730fed9c8abc59c9321132b87476
“PENTAX” VIDEO DUODENOSCOPE
TW: “賓得”電子十二指腸內視鏡
Taiwan·Risk Class 2·MD·HOYA CORPORATION PENTAX MIYAGI FACTORY·Registered Mar 10, 2015 – Mar 10, 2025ExpiredRegistration details
- Analysis ID
- bfeb730fed9c8abc59c9321132b87476
- License Form
- Ministry of Health Medical Device Import No. 027130
- Customs Code
- DHA05602713000
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-urology devices
- Product Type (Level 2)
- H1500 endoscope and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 10, 2015
- Expiry Date
- Mar 10, 2025
About this record
Access comprehensive regulatory information for “PENTAX” VIDEO DUODENOSCOPE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bfeb730fed9c8abc59c9321132b87476 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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