AccessGUDID - DEVICE: NA (00816576028948)

GUDID

Device Identifier (DI) Information

Brand Name: NA
Version or Model: E130BX
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: E130BX
Company Name: HARDY DIAGNOSTICS

Primary DI Number: 00816576028948
Issuing Agency: GS1
Commercial Distribution End Date: December 20, 2024
Device Count: 100
Labeler D-U-N-S® Number*: 039981550 *Terms of Use

Device Description: THAYER MARTIN, MODIFIED Hardy Diagnostics Modified Thayer Martin (MTM) is a selective medium used in qualitative procedures for the isolation of Neisseria gonorrhoeae with suppression of most other gram-negative diplococci, gram-negative bacilli, gram-positive organisms, and yeast.

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?
58585	Differential/selective agar culture medium IVD	An agar 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 on the same medium by appearance (e.g., colour, shape, growth pattern). 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
JTY	Culture Media, For Isolation Of Pathogenic Neisseria

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K934331	000

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 8 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: aa13ac02-4afd-4d55-bb2b-a17ae015ef5a
Public Version Date: December 23, 2024
Public Version Number: 2
DI Record Publish Date: March 31, 2020