"A&T"Laboratory Automation System (Non-Sterile)Discrete photometric chemistry analyzer for clinical use (Non-Sterile)
Taiwan·Risk Class 1·MD·A&T CORPORATION, ESASHI WORKS·Registered Oct 18, 2021 – Oct 31, 2022Cancelled- Analysis ID
- 0e74f770bd486e251051173d27db5e61
- License Form
- Ministry of Health Medical Device Import Registration No. a00005
- Customs Code
- DHA084a0000507
- Manufacturer
- A&T CORPORATION, ESASHI WORKS
- Manufacturer Country
- Japan
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A2160 Individual photometric chemistry analyzer for clinical use
- Registration Date
- Oct 18, 2021
- Expiry Date
- Oct 31, 2022
- Cancellation Date
- Oct 27, 2021
- Status
- Logged out
- Reason
- 醫療器材商自請註銷;;未展延而逾期者
Access comprehensive regulatory information for "A&T"Laboratory Automation System (Non-Sterile)Discrete photometric chemistry analyzer for clinical use (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0e74f770bd486e251051173d27db5e61 and manufactured by A&T CORPORATION, ESASHI WORKS. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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.