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Benq Medical Technology Corp

⚠️ Moderate Risk

FEI: 3009785506 • Taipei • TAIWAN

FEI

FEI Number

3009785506

📍

Location

Taipei

🇹🇼

Country

TAIWAN
🏢

Address

NO 46, 7 Fl, Zhou-Street; Neihu Distric, Taipei, , Taiwan

Moderate Risk

FDA Import Risk Assessment

30.2
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

5
Total Refusals
3
Unique Violations
5/3/2013
Latest Refusal
4/8/2013
Earliest Refusal

Score Breakdown

Violation Severity
41.4×40%
Refusal Volume
28.8×30%
Recency
0.0×20%
Frequency
50.0×10%
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

3414×

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).

1182×

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).

5081×

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

DateProductViolationsDivision
5/3/2013
79FSETABLE, OPERATING-ROOM, MANUAL
341REGISTERED
Florida District Office (FLA-DO)
5/3/2013
79FSETABLE, OPERATING-ROOM, MANUAL
341REGISTERED
Florida District Office (FLA-DO)
5/3/2013
79FSYLIGHT, SURGICAL, CEILING MOUNTED
118NOT LISTED
341REGISTERED
Florida District Office (FLA-DO)
4/8/2013
79FSETABLE, OPERATING-ROOM, MANUAL
341REGISTERED
Division of Southeast Imports (DSEI)
4/8/2013
79FSYLIGHT, SURGICAL, CEILING MOUNTED
118NOT LISTED
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Benq Medical Technology Corp's FDA import refusal history?

Benq Medical Technology Corp (FEI: 3009785506) has 5 FDA import refusal record(s) in our database, spanning from 4/8/2013 to 5/3/2013.

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. Benq Medical Technology Corp's FEI number is 3009785506.

What types of violations has Benq Medical Technology Corp received?

Benq Medical Technology Corp 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 Benq Medical Technology Corp come from?

All FDA import refusal data for Benq Medical Technology Corp 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.