Hissin Medizintechnik Gmbh
⚠️ Moderate Risk
FEI: 3005322529 • Frankfurt am Main, Hesse • GERMANY
FEI Number
3005322529
Location
Frankfurt am Main, Hesse
Country
GERMANYAddress
Berner Str. 28, , Frankfurt am Main, Hesse, 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
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/21/2006 | 79MUUSYSTEM, SUCTION, LIPOPLASTY | 237NO PMA | Florida District Office (FLA-DO) |
| 12/21/2006 | 80KYXDISPENSER, LIQUID MEDICATION | 237NO PMA | Florida District Office (FLA-DO) |
| 12/21/2006 | 80KMIMONITOR, BED PATIENT | 237NO PMA | Florida District Office (FLA-DO) |
| 12/21/2006 | 74MKJAUTOMATED EXTERNAL DEFIBRILLATORS (NON-WEARABLE) | 237NO PMA | Florida District Office (FLA-DO) |
| 12/21/2006 | 80FPLINCUBATOR, NEONATAL TRANSPORT | 237NO PMA | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Hissin Medizintechnik Gmbh's FDA import refusal history?
Hissin Medizintechnik Gmbh (FEI: 3005322529) has 5 FDA import refusal record(s) in our database, spanning from 12/21/2006 to 12/21/2006.
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. Hissin Medizintechnik Gmbh's FEI number is 3005322529.
What types of violations has Hissin Medizintechnik Gmbh received?
Hissin Medizintechnik Gmbh 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 Hissin Medizintechnik Gmbh come from?
All FDA import refusal data for Hissin Medizintechnik 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.