AccessGUDID - DEVICE: N/A (00819398021319)

GUDID

Device Identifier (DI) Information

Brand Name: N/A
Version or Model: K28
Commercial Distribution Status: In Commercial Distribution
Catalog Number: K28
Company Name: HARDY DIAGNOSTICS

Primary DI Number: 00819398021319
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 20
Labeler D-U-N-S® Number*: 039981550 *Terms of Use

Device Description: Thio with supplements, 15mL, 20x125mm tube, 20 tubes/pack (Thioglycollate without indicator, with hemin, vitamin K, and calcium carbonate chip as a buffer) For the cultivation of anaerobes and other fastidious bacteria. Filtered to remove dead bacteria and debris.

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?
58586	Basic/simple nutrient broth culture medium IVD	A non-selective, non-differential nutrient broth culture medium intended to be used to for the primary growth and isolation of typically non-fastidious microorganisms from a clinical specimen.	Active	false

FDA Product Code

[?]

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

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 30 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: f13acc80-4fba-4aa5-92f9-3aecced62917
Public Version Date: June 09, 2020
Public Version Number: 1
DI Record Publish Date: June 01, 2020