K38

GUDID 00816576020249

MUELLER HINTON BROTH For the preparation of suspensions for disk diffusion sensitivity testing.

HARDY DIAGNOSTICS

Mueller-Hinton broth antimicrobial susceptibility culture medium IVD
Primary Device ID00816576020249
NIH Device Record Keyea901002-3000-4425-aef0-0e8b890f6599
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberK38
Catalog NumberK38
Company DUNS039981550
Company NameHARDY DIAGNOSTICS
Device Count20
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800-266-2222
Emailtechservice@hardydiagnostics.com
Phone800-266-2222
Emailtechservice@hardydiagnostics.com
Phone800-266-2222
Emailtechservice@hardydiagnostics.com

Operating and Storage Conditions

Storage Environment TemperatureBetween 2 Degrees Celsius and 30 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100816576020249 [Primary]
GS100816576021291 [Unit of Use]

FDA Product Code

JTZCulture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-02

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00816576027439 - QwikID2025-07-01 QwikID H. pylori Rapid Antigen Test is a single use immunochromatographic assay for the qualitative detection of H. pylori antig
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