Taiwan FDA registration 2d37ea99da451ee58d349d203d934c32
TECO Uritek（Non-Sterile）
TW: 醫信 尿液分析儀（未滅菌）
Taiwan·Risk Class 1·MD·TECO DIAGNOSTICS·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- 2d37ea99da451ee58d349d203d934c32
- License Form
- Ministry of Health Medical Device Import Registration No. 004341
- Customs Code
- DHA08400434100
Company information
- Manufacturer
- TECO DIAGNOSTICS
- Manufacturer Country
- United States
- Authorized Representative
- HONEST MEDICAL INC.
Product details
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A2900 Automated Urinalysis System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for TECO Uritek（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 2d37ea99da451ee58d349d203d934c32 and manufactured by TECO DIAGNOSTICS. The authorized representative in Taiwan is HONEST MEDICAL INC..
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.
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