GUDID 00848838002472

REMEL, INC.

Mueller-Hinton agar antimicrobial susceptibility culture medium IVD
Primary Device ID00848838002472
NIH Device Record Key58b65582-3ce3-481f-8959-e703461c2bb8
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberR01624
Company DUNS065769564
Company NameREMEL, INC.
Device Count100
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone8002556730
EmailITechnicalSupport@remel.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100848838002472 [Primary]
GS100848838099908 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

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 Number3
Public Version Date2018-07-06
Device Publish Date2016-09-24

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