Taiwan FDA registration 1f4db5826db61c75c5d8db1452d5ad21
"Medecon" thin implantable infusion seat and catheter set
TW: “美德康”薄型植入式輸液座與導管組
Registration details
- Analysis ID
- 1f4db5826db61c75c5d8db1452d5ad21
- Customs Code
- DHA00602057905
Company information
- Manufacturer Country
- Mexico;;United States
- Authorized Representative
- GOLDEN ERA MEDICAL SUPPLY 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.5965 Subcutaneous implantable intravascular injection port and guide
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Feb 03, 2010
- Expiry Date
- Feb 03, 2030
About this record
Access comprehensive regulatory information for "Medecon" thin implantable infusion seat and catheter set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1f4db5826db61c75c5d8db1452d5ad21 and manufactured by Martech Medical Products, S.de R.L.de C.V.;; MEDICAL COMPONENTS, INC.. The authorized representative in Taiwan is GOLDEN ERA MEDICAL SUPPLY 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