Magnamed Tecnologia Medica S.A.
⚠️ Moderate Risk
FEI: 3010311362 • Sao Paulo, Sp • BRAZIL
FEI Number
3010311362
Location
Sao Paulo, Sp
Country
BRAZILAddress
R Sao Paulino 221, , Sao Paulo, Sp, Brazil
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).
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.
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/10/2015 | 73ONZCONTINUOUS VENTILATOR | Florida District Office (FLA-DO) | |
| 8/22/2014 | 73ONZCONTINUOUS VENTILATOR | Florida District Office (FLA-DO) | |
| 8/22/2014 | 73ONZCONTINUOUS VENTILATOR | Florida District Office (FLA-DO) | |
| 8/16/2013 | 73ONZCONTINUOUS VENTILATOR | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Magnamed Tecnologia Medica S.A.'s FDA import refusal history?
Magnamed Tecnologia Medica S.A. (FEI: 3010311362) has 4 FDA import refusal record(s) in our database, spanning from 8/16/2013 to 8/10/2015.
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. Magnamed Tecnologia Medica S.A.'s FEI number is 3010311362.
What types of violations has Magnamed Tecnologia Medica S.A. received?
Magnamed Tecnologia Medica S.A. has been cited for 4 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 Magnamed Tecnologia Medica S.A. come from?
All FDA import refusal data for Magnamed Tecnologia Medica S.A. 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.