Victor EnLite

The VICTOR EnLite instrument is intended for the quantitative determination of TREC (T-cell receptor excision circle) DNA in blood specimens dried on a filter paper as an aid in screening…

Registry build 21.09.26

The VICTOR EnLite instrument is intended for the quantitative determination of TREC (T-cell receptor excision circle) DNA in blood specimens dried on a filter paper as an aid in screening newborns for severe combined immunodeficiency (SCID) using the polymerase chain reaction (PCR) based EnLite Neonatal TREC kit.

5manufacturers in China registered for this device type
2catalogue numbers in this listing
1510(k) clearance
3recalls on this code

Who Else Makes It

Concentrated in Beijing (1), Zhejiang (1), Jiangsu (1).

Chinese manufacturers registered for FDA product code KHO
Manufacturer City Province Registered as Device types
W.h.p.m. Bioresearch & Technology Co., Ltd. Beijing Beijing Manufacturer 37
Vivachek Biotech (Hangzhou) Co., Ltd. Hangzhou, Zhuji Zhejiang Contract manufacturer 21
Jiangsu Macro & Micro-Test MED-Tech Co., Ltd. Nantong Jiangsu Manufacturer 11
Yantai Addcare Bio-Tech Co., Ltd. Yantai Shandong Contract manufacturer 8
Guangzhou Labsim Biotech Co., Ltd. Guangzhou Guangdong Manufacturer 3

Record

Regulatory record for Victor EnLite
Listed by Wallac OY, Finland
FDA product code KHO
Device type Fluorometer, For Clinical Use
Device class Class 1
Regulation 21 CFR 862.2560
Establishment Complaint-file establishment, Manufacturer, Exporter
Premarket notification Exempt
Record published 2019-03-19
Record revised 2024-08-01 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries serial number
Distribution end date 2024-04-22

Catalogue Numbers

Catalogue numbers for Victor EnLite
Catalogue number Size Status
1420-0220 Withdrawn
1420-0230 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Sofia Quidel Corp. 4
Vitros Ortho-Clinical Diagnostics, Inc. 3
AutoDELFIA Plate processor Wallac OY 2
AutoDELFIA Automatic Immunoassay System Wallac OY 2
Fluorometer, For Clinical Use Guangzhou Labsim Biotech Co., Ltd. 2
Macro & Micro-Test Fluorescence Immunoassay Analyzer Jiangsu Macro & Micro-Test MED-Tech Co., Ltd. 2
AutoDELFIA Sample processor Wallac OY 2
Asfa® Scanner MBD Co., Ltd. 2
VICTOR2 D Wallac OY 2
Seeker™ Baebies Inc. 2
Frend System Nanoentek Inc 2
Carolina Liquid Chemistries Corp. Immunofluorescence Analyzer Ryan Carolina Liquid Chemistries 1

Showing 12 of 34. All products under Fluorometer, For Clinical Use

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K935047 1994-05-23

Recalls

2 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
2017-01-05 Class II Component change control The firm became aware that the ball bushing axels are defective in the GSP instrument. During exposure to humid conditions, there is a risk that the axle material will corrode. Deterioration of the axle can be observed as deposits of corros 24 instruments and 3 spare disk remover modules 2017-08-24
2017-01-05 Class II Component change control The firm became aware that the ball bushing axels are defective in the GSP instrument. During exposure to humid conditions, there is a risk that the axle material will corrode. Deterioration of the axle can be observed as deposits of corros 24 instruments and 3 spare disk remover modules 2017-08-24
2012-01-09 Not classified Nonconforming Material/Component GSP instruments with defective washer modules may cause a false negative screening result being reported for T4, TSH and IRT. For 17-OHP, a false positive result may be generated if the failure occurs for a normal sample. 10 units 2013-03-06

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