Vidas® 3 Software V1.4

VIDAS 3 V1.4 Software

Registry build 21.09.26
16manufacturers in China registered for this device type
1catalogue number
4recalls on this code

Who Else Makes It

Concentrated in Guangdong (5), Jiangsu (3), Zhejiang (2). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code JJE
Manufacturer City Province Registered as Device types
Dirui Industrial Co., Ltd. Changchun Jilin Contract manufacturer 84
Dongguan BAO Kang Dian ZI KE JI Limited Dongguan Guangdong Contract manufacturer 24
Beckman Coulter Laboratory Systems (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 4
Zhejiang Orient Gene Biotech Huzhou Zhejiang Contract manufacturer 86
Biobase Biodustry(Shandong)Co., Ltd. Jinan Shandong Manufacturer 70
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
Shenzhen Yhlo Biotech Co., Ltd. Shenzhen Guangdong Manufacturer 19
Getein Biotech, Inc. Nanjing Jiangsu Manufacturer 19
Beijing Hotgen Biotech Co., Ltd. Beijing Beijing Manufacturer 13
Yantai Addcare Bio-Tech Co., Ltd. Yantai Shandong Contract manufacturer 8
Shenzhen NEW Industries Biomedical Engineering Co., Ltd. Shenzhen Guangdong Manufacturer 4
Shanghai Kehua Laboratory System Co., Ltd. Shanghai Shanghai Manufacturer 4

Showing 12 of 16. All 16 manufacturers in China registered for Analyzer, Chemistry (Photometric, Discrete), For Clinical Use

Record

Regulatory record for Vidas® 3 Software V1.4
Listed by bioMerieux, Inc., United States
FDA product code JJE
Device type Analyzer, Chemistry (Photometric, Discrete), For Clinical Use
Device class Class 1
Regulation 21 CFR 862.2160
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K141133
Record published 2023-07-04

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only

Catalogue Numbers

Catalogue numbers for Vidas® 3 Software V1.4
Catalogue number Size Status
1.4 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Alinity Abbott Medical 283
Architect Abbott Laboratories 115
Alinity Abbott Laboratories 18
Biobase Biobase Biodustry(Shandong)Co., Ltd. 15
Vitros Ortho-Clinical Diagnostics, Inc. 14
Architect Abbott Ireland Diagnostics 8
AU Beckman Coulter, Inc. 7
Alinity Abbott Ireland Diagnostics 6
DxC AU Beckman Coulter, Inc. 6
Chemiluminescence Immunoassay Analyzer Shenzhen Yhlo Biotech Co., Ltd. 6
Automated Chemiluminescent Enzyme Immunoassay Analyzer AIA-CL300 Tosoh Corp. 5
Pictus 500 Clinical chemistry analyzer Diatron Medicinai Instrumentumok Laboratoriumi Diagnosztikai Fejleszto-Gyarto Zartkoruen Mukodo Reszvenytarsasag 4

Showing 12 of 336. All products under Analyzer, Chemistry (Photometric, Discrete), For Clinical Use

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Vidas® 3 Software V1.4
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
bioMerieux, Inc. 510(k) number 2019-10-22 Class II Software design Following Customers complaints, investigations have been initiated on potentially false results obtained on VIDAS 3 with an expired calibration.
Indeed, the calibrations of assays were valid in the calibration menu whereas in fact the cali
738 units 2024-08-06

Recalls

3 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2018-03-01 Class II Nonconforming Material/Component Several complaints were received for invalid calibration with low calibrator S1 while using VIDAS LH. Internal tests confirmed a decrease of the strips signal overtime for specific lots. 5,429 units 2025-12-09
2018-01-04 Class II Device Design Increase of events affecting performance regarding pump clogging and displacement of the color-coded SPR label (DOT). These performance issues could contribute to erroneous results for any assay performed on the VIDAS and mini VIDAS system 1,866 units 2022-04-14
2018-01-04 Class II Device Design Increase of events affecting performance regarding pump clogging and displacement of the color-coded SPR label (DOT). These performance issues could contribute to erroneous results for any assay performed on the VIDAS and mini VIDAS system 1,866 units 2022-04-14

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer