Taiwan FDA registration 3a0a91cfd3b4226baeb1afbf176b0108
"Pentax" ultrasound electronic upper gastrointestinal endoscope
TW: “賓得士”超音波電子式上消化道內視鏡
Taiwan·Risk Class 2·HOYA CORPORATION PENTAX MIYAGI FACTORY·Registered Mar 03, 2010 – Mar 03, 2025ExpiredRegistration details
- Analysis ID
- 3a0a91cfd3b4226baeb1afbf176b0108
- Customs Code
- DHA00602062104
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
- Mar 03, 2010
- Expiry Date
- Mar 03, 2025
About this record
Access comprehensive regulatory information for "Pentax" ultrasound electronic upper gastrointestinal endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3a0a91cfd3b4226baeb1afbf176b0108 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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