NINGBO UNIMED MEDICAL INSTRUMENTCO LTD
⚠️ Moderate Risk
FEI: 3015118887 • Ningbo, Zhejiang • CHINA
FEI Number
3015118887
Location
Ningbo, Zhejiang
Country
CHINAAddress
No 26 Laoshan Road, , Ningbo, Zhejiang, China
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 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.
FAILS STD
The article appears to be a device which is subject to a performance standard established under Section 514 and does not appear to be in all respects in conformity with such standard.
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
Frequently Asked Questions
What is NINGBO UNIMED MEDICAL INSTRUMENTCO LTD's FDA import refusal history?
NINGBO UNIMED MEDICAL INSTRUMENTCO LTD (FEI: 3015118887) has 2 FDA import refusal record(s) in our database, spanning from 3/15/2005 to 9/27/2007.
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. NINGBO UNIMED MEDICAL INSTRUMENTCO LTD's FEI number is 3015118887.
What types of violations has NINGBO UNIMED MEDICAL INSTRUMENTCO LTD received?
NINGBO UNIMED MEDICAL INSTRUMENTCO LTD has been cited for 3 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 NINGBO UNIMED MEDICAL INSTRUMENTCO LTD come from?
All FDA import refusal data for NINGBO UNIMED MEDICAL INSTRUMENTCO LTD 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.