AccessGUDID - DEVICE: BD Veritor™ Plus Laboratory Combo Pack (00382902560708)

GUDID

Device Identifier (DI) Information

Brand Name: BD Veritor™ Plus Laboratory Combo Pack
Version or Model: 256070
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 256070
Company Name: BECTON, DICKINSON AND COMPANY

Primary DI Number: 00382902560708
Issuing Agency: GS1
Commercial Distribution End Date: June 08, 2020
Device Count: 1
Labeler D-U-N-S® Number*: 122561087 *Terms of Use

Device Description: Combo Veritor Reader 2 Hospital Flu Kit

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
49119	Influenza A/B virus antigen IVD, kit, rapid ICT, clinical	A collection of reagents and other associated materials intended to be used for the qualitative and/or (semi-)quantitative detection of antigens from influenza A virus and/or influenza B virus in a clinical specimen within a short period, relative to standard laboratory testing procedures, using an immunochromatographic test (ICT) method [lateral flow test]. This is a rapid test used in the laboratory or in point-of-care analyses. It is not intended to be used for self-testing.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GNX	ANTIGENS, CF (INCLUDING CF CONTROL), INFLUENZA VIRUS A, B, C
GTY	ANTIGENS, ALL GROUPS, STREPTOCOCCUS SPP.

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Storage Environment Temperature: between 15 and 30 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: f5680c37-617e-47e9-89eb-f57426cf8551
Public Version Date: November 01, 2023
Public Version Number: 2
DI Record Publish Date: May 25, 2018