Taiwan FDA registration ba6854aceb042ad834719ac5b68037ef
“RMS” High-Flo Subcutaneous Safety Needle Sets
TW: “瑞普”海福皮下安全注射針組
Taiwan·Risk Class 2·MD·Repro-Med Systems, Inc. dba KORU Medical Systems·Registered Nov 11, 2019 – Nov 11, 2024ExpiredRegistration details
- Analysis ID
- ba6854aceb042ad834719ac5b68037ef
- License Form
- Ministry of Health Medical Device Import No. 032919
- Customs Code
- DHA05603291902
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
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 11, 2019
- Expiry Date
- Nov 11, 2024
About this record
Access comprehensive regulatory information for “RMS” High-Flo Subcutaneous Safety Needle Sets in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ba6854aceb042ad834719ac5b68037ef 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