AccessGUDID - DEVICE: KWIK-STIK™ Plus (10845357010411)

GUDID

Device Identifier (DI) Information

Brand Name: KWIK-STIK™ Plus
Version or Model: 0445UX
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 0445UX
Company Name: MICROBIOLOGICS INC.

Primary DI Number: 10845357010411
Issuing Agency: GS1
Commercial Distribution End Date: August 01, 2020
Device Count: 1
Labeler D-U-N-S® Number*: 060467826 *Terms of Use

Device Description: KWIK-STIK™ Plus B. vulgatus ATCC 8482™

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?
61331	Multiple bacteria species culture isolate identification control IVD, kit	A collection of reagents and other associated materials intended to be used to verify the performance of one or multiple biochemical tests used for the differentiation and/or identification of multiple bacteria species that have been isolated by culture from a clinical specimen.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
JTR	KIT, QUALITY CONTROL FOR CULTURE MEDIA

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes 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: 99c4f107-5613-491e-ab31-5b11846111aa
Public Version Date: August 11, 2020
Public Version Number: 2
DI Record Publish Date: April 30, 2020