AccessGUDID - DEVICE: Gram-Positive Blood Culture (BC-GP) Extraction Tray (00857573006218)

GUDID

Device Identifier (DI) Information

Brand Name: Gram-Positive Blood Culture (BC-GP) Extraction Tray
Version or Model: 20-009-018
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: NANOSPHERE, INC.

Primary DI Number: 00857573006218
Issuing Agency: GS1
Commercial Distribution End Date: December 05, 2019
Device Count: 1
Labeler D-U-N-S® Number*: 164757242 *Terms of Use

Device Description: The Verigene® Gram-Positive Blood Culture Nucleic Acid Test (BC-GP) performed using the sample-to-result Verigene® System is a qualitative, multiplexed in vitro diagnostic test for the simultaneous detection and identification of potentially pathogenic gram-positive bacteria which may cause bloodstream infection (BSI).

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:	Yes
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?
61308	Multiple-type bloodstream pathogen nucleic acid IVD, kit, nucleic acid amplification/mass spectrometry	A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of nucleic acids and/or genes conferring antimicrobial resistance from multiple types of microorgansims associated with bloodstream infection (i.e., bacteria, fungi, and viruses) in a clinical specimen and/or culture isolate, using a nucleic acid amplification/mass spectrometry method.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
NQX	System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococcus Aureus, Direct Specimen
PAM	Gram-Positive Bacteria And Their Resistance Markers

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 2 and 28 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 3525ba02-7325-4879-82fb-5ff62929e74a
Public Version Date: December 04, 2023
Public Version Number: 6
DI Record Publish Date: September 23, 2016