Taiwan FDA registration c58b89538c8551cc3e676fc6ac2a4cde
“PENTAX MEDICAL” VIDEO NASO-PHARYNGO-LARYNGOSCOPE
TW: “賓得醫療”電子式鼻咽喉內視鏡
Taiwan·Risk Class 2·MD·HOYA CORPORATION PENTAX MIYAGI FACTORY·Registered Apr 21, 2017 – Apr 21, 2027ActiveRegistration details
- Analysis ID
- c58b89538c8551cc3e676fc6ac2a4cde
- License Form
- Ministry of Health Medical Device Import No. 029643
- Customs Code
- DHA05602964300
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)
- G ENT device
- Product Type (Level 2)
- G4760 Nasopharyngeal scope (soft or rigid) and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 21, 2017
- Expiry Date
- Apr 21, 2027
About this record
Access comprehensive regulatory information for “PENTAX MEDICAL” VIDEO NASO-PHARYNGO-LARYNGOSCOPE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c58b89538c8551cc3e676fc6ac2a4cde 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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