Taiwan FDA registration e90e943a807dfa02e649b3257242a7d3
“PENTAX” ULTRASOUND UPPER G.I. VIDEOSCOPE
TW: “賓得”超音波電子式上消化道內視鏡
Taiwan·Risk Class 2·MD·HOYA CORPORATION PENTAX MIYAGI FACTORY·Registered May 12, 2016 – May 12, 2026ExpiredRegistration details
- Analysis ID
- e90e943a807dfa02e649b3257242a7d3
- License Form
- Ministry of Health Medical Device Import No. 028577
- Customs Code
- DHA05602857708
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
- May 12, 2016
- Expiry Date
- May 12, 2026
About this record
Access comprehensive regulatory information for “PENTAX” ULTRASOUND UPPER G.I. VIDEOSCOPE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e90e943a807dfa02e649b3257242a7d3 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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