Richter Ltda-Surgical Instrument
⚠️ Moderate Risk
FEI: 3005578139 • Sao Paulo, Sao Paulo • BRAZIL
FEI Number
3005578139
Location
Sao Paulo, Sao Paulo
Country
BRAZILAddress
Rua Boaventura Pereira 143, , Sao Paulo, Sao Paulo, 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).
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 |
|---|---|---|---|
| 8/26/2009 | 78FHQHOLDER, NEEDLE | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 8/26/2009 | 77KCPSYRINGE, ENT | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 8/26/2009 | 74DQRCANNULA, CATHETER | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 9/14/2007 | 80GCXAPPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED | New Orleans District Office (NOL-DO) | |
| 9/14/2007 | 79FZOCHISEL, SURGICAL, MANUAL | 118NOT LISTED | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Richter Ltda-Surgical Instrument's FDA import refusal history?
Richter Ltda-Surgical Instrument (FEI: 3005578139) has 5 FDA import refusal record(s) in our database, spanning from 9/14/2007 to 8/26/2009.
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. Richter Ltda-Surgical Instrument's FEI number is 3005578139.
What types of violations has Richter Ltda-Surgical Instrument received?
Richter Ltda-Surgical Instrument 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 Richter Ltda-Surgical Instrument come from?
All FDA import refusal data for Richter Ltda-Surgical Instrument 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.