Taiwan FDA registration 9dc50d166d1fd52246b3c395b3c73686
“Neotech” Catheter Securement Device (Non-Sterile)
TW: “耐兒泰” 導管固定裝置 (未滅菌)
Taiwan·Risk Class 1·MD·NEOTECH PRODUCTS LLC·Registered Sep 01, 2021 – Sep 01, 2026ActiveRegistration details
- Analysis ID
- 9dc50d166d1fd52246b3c395b3c73686
- License Form
- Ministry of Health Medical Device Import No. 022631
- Customs Code
- DHA09402263104
Company information
- Manufacturer
- NEOTECH PRODUCTS LLC
- Manufacturer Country
- United States
- Authorized Representative
- EXCELSIOR MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of endovascular catheter fixation device (J.5210) of the classification and grading management method of medical equipment.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5210 Endovascular catheter fixation device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 01, 2021
- Expiry Date
- Sep 01, 2026
About this record
Access comprehensive regulatory information for “Neotech” Catheter Securement Device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9dc50d166d1fd52246b3c395b3c73686 and manufactured by NEOTECH PRODUCTS LLC. The authorized representative in Taiwan is EXCELSIOR MEDICAL CO., LTD..
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