Mediplus Ltd
⚠️ Moderate Risk
FEI: 3011308139 • High Wycombe, Buckinghamshire • UNITED KINGDOM
FEI Number
3011308139
Location
High Wycombe, Buckinghamshire
Country
UNITED KINGDOMAddress
Unit 7 The Gateway Centre, Coronation Road, Cressex Business Park, High Wycombe, Buckinghamshire, United Kingdom
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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).
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/24/2013 | 78GBTCATHETER, RECTAL | Florida District Office (FLA-DO) | |
| 7/24/2013 | 78FEDSHEATH, FOR ENDOSCOPE | Florida District Office (FLA-DO) | |
| 7/24/2013 | 78NWQKIT, CATHETER, EXTERNAL, MALE (EXCLUDES HIV TESTING) | Florida District Office (FLA-DO) | |
| 7/24/2013 | 79GCDCONNECTOR, CATHETER | Florida District Office (FLA-DO) | |
| 7/24/2013 | 73OFQANESTHESIA KIT | Florida District Office (FLA-DO) | |
| 7/24/2013 | 80LHISET, I.V. FLUID TRANSER | Florida District Office (FLA-DO) | |
| 7/24/2013 | 73BYGMASK, OXYGEN | Florida District Office (FLA-DO) | |
| 7/24/2013 | 78KODCATHETER, UROLOGICAL | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Mediplus Ltd's FDA import refusal history?
Mediplus Ltd (FEI: 3011308139) has 8 FDA import refusal record(s) in our database, spanning from 7/24/2013 to 7/24/2013.
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. Mediplus Ltd's FEI number is 3011308139.
What types of violations has Mediplus Ltd received?
Mediplus Ltd has been cited for 2 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 Mediplus Ltd come from?
All FDA import refusal data for Mediplus 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.