Perouse Medical
✅ Low Risk
FEI: 3004160911 • Irigny, Rhone • FRANCE
FEI Number
3004160911
Location
Irigny, Rhone
Country
FRANCEAddress
135 Route Neuve, , Irigny, Rhone, France
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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
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 |
|---|---|---|---|
| 12/9/2010 | 87MAXORTHOSIS, SPINAL INTERVERTEBRAL FUSION | 341REGISTERED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Perouse Medical's FDA import refusal history?
Perouse Medical (FEI: 3004160911) has 1 FDA import refusal record(s) in our database, spanning from 12/9/2010 to 12/9/2010.
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. Perouse Medical's FEI number is 3004160911.
What types of violations has Perouse Medical received?
Perouse Medical 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 Perouse Medical come from?
All FDA import refusal data for Perouse Medical 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.