Taiwan FDA registration 24738385e6a9b0e7a94a153370179c84
Chungdo Automated urinalysis system (Non-Sterile)
TW: 長島 自動尿液分析系統 (未滅菌)
Taiwan·Risk Class 1·MD·CHUNGDO PHARM. CO., LTD·Registered Jan 20, 2022 – Oct 31, 2023CancelledRegistration details
- Analysis ID
- 24738385e6a9b0e7a94a153370179c84
- License Form
- Ministry of Health Medical Device Import Registration No. a00034
- Customs Code
- DHA084a0003401
Company information
- Manufacturer
- CHUNGDO PHARM. CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- HORNG-YIH INSTRUMENT A COMPANY LIMITED
Product details
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A2900 Automated Urinalysis System
Dates and status
- Registration Date
- Jan 20, 2022
- Expiry Date
- Oct 31, 2023
- Cancellation Date
- Feb 10, 2023
Cancellation information
- Status
- Logged out
About this record
Access comprehensive regulatory information for Chungdo Automated urinalysis system (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 24738385e6a9b0e7a94a153370179c84 and manufactured by CHUNGDO PHARM. CO., LTD. The authorized representative in Taiwan is HORNG-YIH INSTRUMENT A COMPANY LIMITED.
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