Taiwan FDA registration baaa0ca1c2b9e8e0639f95f51553c9c3
“RMS” Precision Flow Rate Tubing Set
TW: “瑞普”普立森流速管
Registration details
- Analysis ID
- baaa0ca1c2b9e8e0639f95f51553c9c3
- License Form
- Ministry of Health Medical Device Import No. 033031
- Customs Code
- DHA05603303100
Company information
- Manufacturer
- Repro-Med Systems, Inc. dba KORU Medical Systems
- Manufacturer Country
- United States
- Authorized Representative
- GIRAFFES PHARMACEUTICAL COMPANY 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)
- J5440 Intravascular infusion sleeve
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 14, 2019
- Expiry Date
- Nov 14, 2024
About this record
Access comprehensive regulatory information for “RMS” Precision Flow Rate Tubing Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number baaa0ca1c2b9e8e0639f95f51553c9c3 and manufactured by Repro-Med Systems, Inc. dba KORU Medical Systems. The authorized representative in Taiwan is GIRAFFES PHARMACEUTICAL COMPANY 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