BIOBEAT TECHNOLOGIES, LTD.
⚠️ Moderate Risk
FEI: 3015455735 • Petach Tikva, HAMERKAZ • ISRAEL
FEI Number
3015455735
Location
Petach Tikva, HAMERKAZ
Country
ISRAELAddress
26 Magshimim St. Ste 20, , Petach Tikva, HAMERKAZ, Israel
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 |
|---|---|---|---|
| 11/2/2020 | 74DXNSYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE | Division of Northeast Imports (DNEI) | |
| 11/2/2020 | 74DXNSYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE | Division of Northeast Imports (DNEI) | |
| 11/2/2020 | 74DXNSYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is BIOBEAT TECHNOLOGIES, LTD.'s FDA import refusal history?
BIOBEAT TECHNOLOGIES, LTD. (FEI: 3015455735) has 3 FDA import refusal record(s) in our database, spanning from 11/2/2020 to 11/2/2020.
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. BIOBEAT TECHNOLOGIES, LTD.'s FEI number is 3015455735.
What types of violations has BIOBEAT TECHNOLOGIES, LTD. received?
BIOBEAT TECHNOLOGIES, LTD. 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 BIOBEAT TECHNOLOGIES, LTD. come from?
All FDA import refusal data for BIOBEAT TECHNOLOGIES, 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.