ImportRefusal LogoImportRefusal

Gevenmed Sa

✅ Low Risk

FEI: 3004501760 • Caracas, D.F. • VENEZUELA

FEI

FEI Number

3004501760

📍

Location

Caracas, D.F.

🇻🇪

Country

VENEZUELA
🏢

Address

Centro Comercial Macaracuay Plaza, , Caracas, D.F., Venezuela

Low Risk

FDA Import Risk Assessment

23.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
8/7/2006
Latest Refusal
8/7/2006
Earliest Refusal

Score Breakdown

Violation Severity
30.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

3414×

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
8/7/2006
74MLOELECTROCARDIOGRAPH, AMBULATORY WITH ANALYSIS ALGORITHM
341REGISTERED
Florida District Office (FLA-DO)
8/7/2006
74MLOELECTROCARDIOGRAPH, AMBULATORY WITH ANALYSIS ALGORITHM
341REGISTERED
Florida District Office (FLA-DO)
8/7/2006
74MLOELECTROCARDIOGRAPH, AMBULATORY WITH ANALYSIS ALGORITHM
341REGISTERED
Florida District Office (FLA-DO)
8/7/2006
74MLOELECTROCARDIOGRAPH, AMBULATORY WITH ANALYSIS ALGORITHM
341REGISTERED
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Gevenmed Sa's FDA import refusal history?

Gevenmed Sa (FEI: 3004501760) has 4 FDA import refusal record(s) in our database, spanning from 8/7/2006 to 8/7/2006.

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. Gevenmed Sa's FEI number is 3004501760.

What types of violations has Gevenmed Sa received?

Gevenmed Sa 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 Gevenmed Sa come from?

All FDA import refusal data for Gevenmed Sa 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.