Medtronic Perfusion Systems
⚠️ Moderate Risk
FEI: 1000116158 • Brooklyn Park, MN • UNITED STATES
FEI Number
1000116158
Location
Brooklyn Park, MN
Country
UNITED STATESAddress
7611 Northland Dr N, , Brooklyn Park, MN, United States
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
NO PMA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/3/2016 | 74DTNRESERVOIR, BLOOD, CARDIOPULMONARY BYPASS | 508NO 510(K) | Chicago District Office (CHI-DO) |
| 7/17/2014 | 74DTNRESERVOIR, BLOOD, CARDIOPULMONARY BYPASS | 237NO PMA | Atlanta District Office (ATL-DO) |
| 7/17/2014 | 74DTNRESERVOIR, BLOOD, CARDIOPULMONARY BYPASS | 237NO PMA | Atlanta District Office (ATL-DO) |
| 7/17/2014 | 74DTZOXYGENATOR, CARDIOPULMONARY BYPASS | 237NO PMA | Atlanta District Office (ATL-DO) |
| 7/17/2014 | 74DTZOXYGENATOR, CARDIOPULMONARY BYPASS | 237NO PMA | Atlanta District Office (ATL-DO) |
| 7/17/2014 | 74DTZOXYGENATOR, CARDIOPULMONARY BYPASS | 237NO PMA | Atlanta District Office (ATL-DO) |
| 7/17/2014 | 74DTZOXYGENATOR, CARDIOPULMONARY BYPASS | 237NO PMA | Atlanta District Office (ATL-DO) |
| 7/17/2014 | 74DTZOXYGENATOR, CARDIOPULMONARY BYPASS | 237NO PMA | Atlanta District Office (ATL-DO) |
| 7/17/2014 | 74DTZOXYGENATOR, CARDIOPULMONARY BYPASS | 237NO PMA | Atlanta District Office (ATL-DO) |
| 7/17/2014 | 74DTNRESERVOIR, BLOOD, CARDIOPULMONARY BYPASS | 237NO PMA | Atlanta District Office (ATL-DO) |
Frequently Asked Questions
What is Medtronic Perfusion Systems's FDA import refusal history?
Medtronic Perfusion Systems (FEI: 1000116158) has 10 FDA import refusal record(s) in our database, spanning from 7/17/2014 to 11/3/2016.
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. Medtronic Perfusion Systems's FEI number is 1000116158.
What types of violations has Medtronic Perfusion Systems received?
Medtronic Perfusion Systems 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 Medtronic Perfusion Systems come from?
All FDA import refusal data for Medtronic Perfusion Systems 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.