Taiwan FDA registration 36684dc7bc5b478c65a2424fd52ea572
Endo-Upex Injection Needle P
TW: “安朵優倍斯”一次性內視鏡使用注射針
Taiwan·Risk Class 2·MD·UPEX-MED CO., LTD.·Registered May 25, 2021 – May 25, 2026ExpiredRegistration details
- Analysis ID
- 36684dc7bc5b478c65a2424fd52ea572
- License Form
- Ministry of Health Medical Device Import No. 034566
- Customs Code
- DHA05603456602
Company information
- Manufacturer
- UPEX-MED CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MedPower Medical Co., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H4300 Electrosurgical device for endoscopes and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 25, 2021
- Expiry Date
- May 25, 2026
About this record
Access comprehensive regulatory information for Endo-Upex Injection Needle P in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 36684dc7bc5b478c65a2424fd52ea572 and manufactured by UPEX-MED CO., LTD.. The authorized representative in Taiwan is MedPower Medical Co., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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