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Mednet Gmbh

⚠️ Moderate Risk

FEI: 3006004429 • Munster, North Rhine-Westphalia • GERMANY

FEI

FEI Number

3006004429

📍

Location

Munster, North Rhine-Westphalia

🇩🇪

Country

GERMANY
🏢

Address

Borkstr. 10, , Munster, North Rhine-Westphalia, Germany

Moderate Risk

FDA Import Risk Assessment

41.3
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

2
Total Refusals
1
Unique Violations
12/19/2022
Latest Refusal
10/18/2021
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
17.7×30%
Recency
31.4×20%
Frequency
17.1×10%
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

5082×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
12/19/2022
83QLWCOVID-19 TEST HOME COLLECTION KIT DEVICES
508NO 510(K)
Division of Southeast Imports (DSEI)
10/18/2021
83QOFMULTI-TARGET RESPIRATORY SPECIMEN NUCLEIC ACID TEST INCLUDING SARS-COV-2 AND OTHER MICROBIAL AGENTS
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Mednet Gmbh's FDA import refusal history?

Mednet Gmbh (FEI: 3006004429) has 2 FDA import refusal record(s) in our database, spanning from 10/18/2021 to 12/19/2022.

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. Mednet Gmbh's FEI number is 3006004429.

What types of violations has Mednet Gmbh received?

Mednet Gmbh 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 Mednet Gmbh come from?

All FDA import refusal data for Mednet Gmbh 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.