Taiwan FDA registration 7f66b1123e1cc7ee38a591d4f50b44de
"Pentax" Stella uses a tourniquet single-use
TW: “賓得”施黛拉一次性使用止血夾
Taiwan·Risk Class 2·JIANGSU VEDKANG MEDICAL SCIENCE & TECHNOLOGY CO., LTD.·Registered Oct 31, 2022 – Oct 31, 2027ActiveRegistration details
- Analysis ID
- 7f66b1123e1cc7ee38a591d4f50b44de
- Customs Code
- DHA09200141708
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
- Oct 31, 2022
- Expiry Date
- Oct 31, 2027
About this record
Access comprehensive regulatory information for "Pentax" Stella uses a tourniquet single-use in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7f66b1123e1cc7ee38a591d4f50b44de 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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