Taiwan FDA registration c6effab451af66b2d0db0e835a54ca6f
"Medelai" intravenous indwelling needle
TW: “美德萊”靜脈留置針
Taiwan·Risk Class 2·Yangzhou Medline Industry Co., Ltd.·Registered Jul 31, 2019 – Jul 31, 2024ExpiredRegistration details
- Analysis ID
- c6effab451af66b2d0db0e835a54ca6f
- Customs Code
- DHA09200105401
Company information
- Manufacturer
- Yangzhou Medline Industry Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- EAFAN ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5570 Subcutaneous single-chamber needle
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jul 31, 2019
- Expiry Date
- Jul 31, 2024
About this record
Access comprehensive regulatory information for "Medelai" intravenous indwelling needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c6effab451af66b2d0db0e835a54ca6f and manufactured by Yangzhou Medline Industry Co., Ltd.. The authorized representative in Taiwan is EAFAN ENTERPRISE 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.
Free DatabasePowered by Pure Global AI89,000+ Devices