AccessGUDID - DEVICE: NovaSeq™ 6000Dx Library Tube, 24 pack (00816270020583)

GUDID

Device Identifier (DI) Information

Brand Name: NovaSeq™ 6000Dx Library Tube, 24 pack
Version or Model: 20062291
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 20062291
Company Name: ILLUMINA, INC.

Primary DI Number: 00816270020583
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 033305264 *Terms of Use

Device Description: The Illumina NovaSeq™ 6000Dx Library Tubes, 24 pack are intended to hold sample libraries for sequencing with NovaSeq™ 6000Dx S2 or S4 reagent kits and validated assays. The tubes are boxed together in one box, 20060177, NovaSeq™ 6000Dx Library Tubes Pk, which is labeled with the same Device Identifier.

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:	Yes
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?
62173	Nucleic acid sequencing reagent kit IVD	A collection of reagents and other associated materials intended to be used on-board a nucleic acid sequencing instrument for the genetic analysis of a clinical specimen. It typically consists of buffers, primers, enzymes (e.g., DNA polymerase, DNA ligase) and deoxynucleotides (dNTPs). It does not contain analyte-specific reagents and is not intended to be used for whole genome or complementary deoxyribonucleic acid (cDNA) library construction.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
PFT	Reagents For Molecular Diagnostic Test Systems

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
Handling Environment Temperature: between 15 and 30 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: b356bacf-65a2-4430-8f87-fde4ebc3d718
Public Version Date: October 26, 2022
Public Version Number: 1
DI Record Publish Date: October 18, 2022