AccessGUDID - DEVICE: illumigene Mycoplasma External Control Kit (00840733101144)

GUDID

Device Identifier (DI) Information

Brand Name: illumigene Mycoplasma External Control Kit
Version or Model: 279940
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 279940
Company Name: MERIDIAN BIOSCIENCE, INC.

Primary DI Number: 00840733101144
Issuing Agency: GS1
Commercial Distribution End Date: July 25, 2018
Device Count: 1
Labeler D-U-N-S® Number*: 092815364 *Terms of Use

Device Description: The illumigene Mycoplasma External Control Kit contains Positive and Negative Control Reagents for use with the illumigene Mycoplasma test kit. External controls are used as part of a routine quality control program. External controls are used as part of a routine quality control program.

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):	Yes
Over the Counter (OTC):	No
Kit:	Yes
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?
47327	Mycoplasma pneumoniae nucleic acid IVD, control	A material which is used to verify the performance of an assay intended to be used for the qualitative and/or quantitative detection of nucleic acid from Mycoplasma pneumoniae bacteria in a clinical specimen.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
OOI	Real Time Nucleic Acid Amplification System
OZX	Mycoplasma Pneumoniae Dna Assay System

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
Handling Environment Temperature: between 2 and 8 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: ed74a0b5-f96e-4e2a-aabe-834adb73f105
Public Version Date: July 16, 2020
Public Version Number: 3
DI Record Publish Date: September 23, 2016