Taiwan FDA registration 06f97df0687d3fcd797761a2dc30ff37
"Pentax Medical" electronic nasopharyngeal endoscope
TW: “賓得醫療”電子式鼻咽喉內視鏡
Taiwan·Risk Class 2·DIGITAL ENDOSCOPY GMBH;; HOYA Corporation.·Registered Nov 26, 2019 – Nov 26, 2029ActiveRegistration details
- Analysis ID
- 06f97df0687d3fcd797761a2dc30ff37
- Customs Code
- DHA05603300904
Company information
- Manufacturer
- DIGITAL ENDOSCOPY GMBH;; HOYA Corporation.
- Manufacturer Country
- Germany;;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 Science
- Product Type (Level 2)
- G.4760 Nasopharyngeal scopes (soft or rigid) and their accessories
- Import Information
- import
Dates and status
- Registration Date
- Nov 26, 2019
- Expiry Date
- Nov 26, 2029
About this record
Access comprehensive regulatory information for "Pentax Medical" electronic nasopharyngeal endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 06f97df0687d3fcd797761a2dc30ff37 and manufactured by DIGITAL ENDOSCOPY GMBH;; HOYA Corporation.. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).
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