Taiwan FDA registration 1fbd910dec0340a676720869f82c97b3
"Pentax" Stella uses a slicer in a single pass
TW: “賓得”施黛拉單次使用切片鉗
Taiwan·Risk Class 2·JIANGSU VEDKANG MEDICAL SCIENCE & TECHNOLOGY CO., LTD.·Registered Apr 26, 2022 – Apr 26, 2027ActiveRegistration details
- Analysis ID
- 1fbd910dec0340a676720869f82c97b3
- Customs Code
- DHA09200135104
Company information
- Manufacturer Country
- China
- Authorized Representative
- PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE)
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1500 Internal Scope and its accessories
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Apr 26, 2022
- Expiry Date
- Apr 26, 2027
About this record
Access comprehensive regulatory information for "Pentax" Stella uses a slicer in a single pass in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1fbd910dec0340a676720869f82c97b3 and manufactured by JIANGSU VEDKANG MEDICAL SCIENCE & TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).
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