AccessGUDID - DEVICE: N/A (00819398026352)

GUDID

Device Identifier (DI) Information

Brand Name: N/A
Version or Model: Z24
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: Z24
Company Name: HARDY DIAGNOSTICS

Primary DI Number: 00819398026352
Issuing Agency: GS1
Commercial Distribution End Date: February 12, 2021
Device Count: 20
Labeler D-U-N-S® Number*: 039981550 *Terms of Use

Device Description: Rapid DNase Broth, Tube Flat Bottom 13x100mm EP Glass, 0.5ml fill, order by the package of 20 Hardy Diagnostics Rapid DNase Broth is recommended for the detection of deoxyribonuclease (DNase) activity of gram-negative and gram-positive bacteria, particularly Staphylococcus aureus, Moraxella catarrhalis, and Serratia marcescens. Positives turn the broth a milky white.

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):	No
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?
58684	Differential/selective broth culture medium IVD	A broth culture medium intended to be used to promote the selective growth of a microbial species with specific characteristics (e.g., antibiotic resistance, ability to utilize, synthesize specific metabolites) and/or distinguish between microbial species growing in the same medium. It typically contains substances to inhibit the growth of commensal or contaminating microorganisms (e.g., antimicrobials, dyes, salts) and/or dyes or chemical indicators for differentiation.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
JSH	Culture Media, Non-Selective And Differential

FDA Premarket Submission

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

Device Exempt from Premarket Submission: Yes 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 8 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: b4d2ead9-b19e-484e-8dfa-cf86468dde1d
Public Version Date: February 15, 2021
Public Version Number: 3
DI Record Publish Date: June 16, 2020