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CATHVISION APS

⚠️ Moderate Risk

FEI: 3030129257 • Copenhagen N, Hovedstaden • DENMARK

FEI

FEI Number

3030129257

📍

Location

Copenhagen N, Hovedstaden

🇩🇰

Country

DENMARK
🏢

Address

Noerrebro, Titangade 11, Copenhagen N, Hovedstaden, Denmark

Moderate Risk

FDA Import Risk Assessment

36.8
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
2/28/2024
Latest Refusal
2/28/2024
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
11.2×30%
Recency
62.2×20%
Frequency
10.0×10%
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

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

Refusal History

DateProductViolationsDivision
2/28/2024
78KNXCOLLECTOR, URINE, (AND ACCESSORIES) FOR INDWELLING CATHETER
118NOT LISTED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is CATHVISION APS's FDA import refusal history?

CATHVISION APS (FEI: 3030129257) has 1 FDA import refusal record(s) in our database, spanning from 2/28/2024 to 2/28/2024.

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. CATHVISION APS's FEI number is 3030129257.

What types of violations has CATHVISION APS received?

CATHVISION APS 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 CATHVISION APS come from?

All FDA import refusal data for CATHVISION APS 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.