Taiwan FDA registration b9a513bf3d549c51d679f7a12b40e295
“PENTX” ELECTRO-SURGICAL KNIFE
TW: “賓得”電燒手術刀器械
Taiwan·Risk Class 2·MD·HOYA CORPORATION PENTAX YAMAGATA FACTORY·Registered May 12, 2016 – May 12, 2021ExpiredRegistration details
- Analysis ID
- b9a513bf3d549c51d679f7a12b40e295
- License Form
- Ministry of Health Medical Device Import No. 028578
- Customs Code
- DHA05602857800
Company information
- Manufacturer
- HOYA CORPORATION PENTAX YAMAGATA 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)
- H4300 Electrocutors for endoscopes and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 12, 2016
- Expiry Date
- May 12, 2021
About this record
Access comprehensive regulatory information for “PENTX” ELECTRO-SURGICAL KNIFE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b9a513bf3d549c51d679f7a12b40e295 and manufactured by HOYA CORPORATION PENTAX YAMAGATA FACTORY. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).
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