GenePOC™ Carba

The GenePOC™ Carba assay, performed on the revogene™ instrument, is a qualitative in vitro diagnostic test designed for the detection and differentiation of the blaKPC, blaNDM, blaVIM,…

Registry build 21.09.26

The GenePOC™ Carba assay, performed on the revogene™ instrument, is a qualitative in vitro diagnostic test designed for the detection and differentiation of the blaKPC, blaNDM, blaVIM, blaOXA-48-like, and blaIMP gene sequences associated with carbapenem-non-susceptible pure colonies of Enterobacteriaceae, Acinetobacter baumannii, or Pseudomonas aeruginosa, when grown on blood agar or MacConkey agar. The test utilizes automated real-time Polymerase Chain Reaction (PCR). The GenePOC Carba assay should be used in conjunction with other laboratory tests including phenotypic antimicrobial susceptibility testing. A negative GenePOC Carba assay result does not preclude the presence of other resistance mechanisms. The GenePOC Carba assay is intended as an aid for infection control in the detection of carbapenem-non-susceptible bacteria that colonize patients in healthcare settings. The identification of a blaIMP, blaNDM or blaVIM metallo-B-lactamase gene (i.e., the genes that encode the IMP, NDM and VIM metallo-B-lactamases, respectively) may be used as an aid to clinicians in determining appropriate therapeutic strategies for patients with known or suspected carbapenem non-susceptible infections.

15manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Jiangsu (4), Shandong (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 OOI
Manufacturer City Province Registered as Device types
Zhejiang Orient Gene Biotech Huzhou Zhejiang Contract manufacturer 86
Guangzhou Four E’s Scientific Co., Ltd. Guangzhou Guangdong Contract manufacturer 61
Sanmina Kunshan Jiangsu Contract manufacturer 15
Biobase Biodustry(Shandong)Co., Ltd. Jinan Shandong Manufacturer 70
Infitek Co., Ltd. Shanghai Shanghai Manufacturer 49
Labpeak Co., Ltd. Jinan Shandong Manufacturer 43
Scitek Global Co., Ltd. Jinan Shandong Manufacturer 43
Bioteke Corporation (Wuxi) Co., Ltd. Wuxi Jiangsu Manufacturer 21
Getein Biotech, Inc. Nanjing Jiangsu Manufacturer 19
Xian Tianlong Science AND Technology Co., Ltd. Xi’An Shaanxi Manufacturer 8
Hangzhou Bioer Technology Co., Ltd. Hangzhou Zhejiang Manufacturer 6
Sansure Biotech Inc. Changsha Hunan Manufacturer 4

Showing 12 of 15. All 15 manufacturers in China registered for Real Time Nucleic Acid Amplification System

Record

Regulatory record for GenePOC™ Carba
Listed by Genepoc, Inc., Canada
FDA product code OOI
Device type Real Time Nucleic Acid Amplification System
Device class Class 2
Regulation 21 CFR 862.2570
Record published 2019-05-24
Record revised 2021-10-01 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Storage Storage environment temperature 2 to 25 °C
Distribution end date 2021-09-30

Catalogue Numbers

Catalogue numbers for GenePOC™ Carba
Catalogue number Size Status
133499 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
GeneXpert Dx System Cepheid 37
Alinity m Abbott Molecular, Inc. 20
GeneXpert Infinity-80 System Cepheid 13
Fluorescence Quantitative PCR Detection System Anitoa Biotechnology(Hangzhou)Co., Ltd. 12
GeneXpert® Cepheid 10
Certified Pre-Owned GeneXpert Dx System Cepheid 10
Bioer GeneExplorer Thermal Cycler Hangzhou Bioer Technology Co., Ltd. 7
m2000 Abbott Molecular, Inc. 5
GeneXpert Infinity-48s System Cepheid 5
Panther Fusion® Hologic, Inc. 4
Bioer LineGene 9600 Plus Fluorescent Quantitative Detection System Hangzhou Bioer Technology Co., Ltd. 4
Bioer QuantGene 9600 Fluorescent Quantitative Detection System Hangzhou Bioer Technology Co., Ltd. 3

Showing 12 of 188. All products under Real Time Nucleic Acid Amplification System

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K170558 2017-05-25

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