Taiwan FDA registration 835247f54e4e7992667d3b52a76429d9
“PENTAX” VIDEO SMALL BOWEL ENTEROSCOPE
TW: “賓得”電子小腸內視鏡
Taiwan·Risk Class 2·MD·HOYA CORPORATION PENTAX MIYAGI FACTORY·Registered Mar 12, 2015 – Mar 12, 2020CancelledRegistration details
- Analysis ID
- 835247f54e4e7992667d3b52a76429d9
- License Form
- Ministry of Health Medical Device Import No. 027134
- Customs Code
- DHA05602713408
Company information
- Manufacturer
- HOYA CORPORATION PENTAX MIYAGI FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE)
Product details
- 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 12, 2015
- Expiry Date
- Mar 12, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “PENTAX” VIDEO SMALL BOWEL ENTEROSCOPE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 835247f54e4e7992667d3b52a76429d9 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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