Philips Medical Systems DMC GmbH
⚠️ Moderate Risk
FEI: 3003768251 • Hamburg, Hamburg • GERMANY
FEI Number
3003768251
Location
Hamburg, Hamburg
Country
GERMANYAddress
Development And Manufacturing Ctr., Rontgenstr. 24, Hamburg, Hamburg, Germany
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
Frequently Asked Questions
What is Philips Medical Systems DMC GmbH's FDA import refusal history?
Philips Medical Systems DMC GmbH (FEI: 3003768251) has 2 FDA import refusal record(s) in our database, spanning from 10/28/2011 to 4/8/2013.
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. Philips Medical Systems DMC GmbH's FEI number is 3003768251.
What types of violations has Philips Medical Systems DMC GmbH received?
Philips Medical Systems DMC GmbH 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 Philips Medical Systems DMC GmbH come from?
All FDA import refusal data for Philips Medical Systems DMC GmbH 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.