Taiwan FDA registration c29baf3244676a5586cf1489157b5be8
"Plusrite" implantable infusion seat special safety perfusion needle
TW: “普羅斯”植入式輸液座專用安全灌注針
Registration details
- Analysis ID
- c29baf3244676a5586cf1489157b5be8
- Customs Code
- DHA00602294909
Company information
- Manufacturer
- PEROUSE MEDICAL
- Manufacturer Country
- France
- Authorized Representative
- AMED 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.5440 血管內輸液套
- Import Information
- import
Dates and status
- Registration Date
- Dec 05, 2011
- Expiry Date
- Dec 05, 2026
About this record
Access comprehensive regulatory information for "Plusrite" implantable infusion seat special safety perfusion needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c29baf3244676a5586cf1489157b5be8 and manufactured by PEROUSE MEDICAL. The authorized representative in Taiwan is AMED 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