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Uritest Medical Electronics Co Ltd

✅ Low Risk

FEI: 3006125765 • Guilin, Guangxi • CHINA

FEI

FEI Number

3006125765

📍

Location

Guilin, Guangxi

🇨🇳

Country

CHINA
🏢

Address

No 4 E Alley Jiuhua Road, , Guilin, Guangxi, China

Low Risk

FDA Import Risk Assessment

19.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

2
Total Refusals
1
Unique Violations
3/14/2011
Latest Refusal
3/14/2011
Earliest Refusal

Score Breakdown

Violation Severity
30.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

3412×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

Refusal History

DateProductViolationsDivision
3/14/2011
78MNVSTRIP, DIALYSATE PH INDICATOR
341REGISTERED
New England District Office (NWE-DO)
3/14/2011
81KQGINSTRUMENT, COAGULATION
341REGISTERED
New England District Office (NWE-DO)

Frequently Asked Questions

What is Uritest Medical Electronics Co Ltd's FDA import refusal history?

Uritest Medical Electronics Co Ltd (FEI: 3006125765) has 2 FDA import refusal record(s) in our database, spanning from 3/14/2011 to 3/14/2011.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Uritest Medical Electronics Co Ltd's FEI number is 3006125765.

What types of violations has Uritest Medical Electronics Co Ltd received?

Uritest Medical Electronics Co Ltd has been cited for 1 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about Uritest Medical Electronics Co Ltd come from?

All FDA import refusal data for Uritest Medical Electronics Co Ltd is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.