Taiwan FDA registration 62076cdf088aa6e5285a49796f9b8825
“Streck” ESR-Vacuum Tubes
TW: “斯垂克” 真空紅血球沉降速率測定試管
Taiwan·Risk Class 2·MD·LINE·Registered Oct 30, 2014 – Oct 30, 2019CancelledRegistration details
- Analysis ID
- 62076cdf088aa6e5285a49796f9b8825
- License Form
- Ministry of Health Medical Device Import No. 026724
- Customs Code
- DHA05602672401
Company information
- Manufacturer
- LINE
- Manufacturer Country
- United States
- Authorized Representative
- RECHI CO., LTD.
Product details
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1675 Blood Sample Collection Device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 30, 2014
- Expiry Date
- Oct 30, 2019
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “Streck” ESR-Vacuum Tubes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 62076cdf088aa6e5285a49796f9b8825 and manufactured by LINE. The authorized representative in Taiwan is RECHI 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