AccessGUDID - DEVICE: ABBOTT PRISM (00380740007904)

GUDID

Device Identifier (DI) Information

Brand Name: ABBOTT PRISM
Version or Model: 5A07-01
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 05A0701
Company Name: ABBOTT LABORATORIES

Primary DI Number: 00380740007904
Issuing Agency: GS1
Commercial Distribution End Date: March 21, 2023
Device Count: 112
Labeler D-U-N-S® Number*: 079226220 *Terms of Use

Device Description: ABBOTT PRISM Reaction Trays

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:	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?
56701	Chemiluminescent immunoassay analyser IVD	An electrically-powered automated or semi-automated laboratory instrument intended to be used for the qualitative and/or quantitative in vitro determination of chemical and/or biological markers (e.g., protein, drug, hormone, microbial toxin) in a clinical specimen, using an immunological method that utilizes a chemiluminescent detection system together with sample processing, data processing and/or data display software.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MZA	TEST,EQUIPMENT,AUTOMATED BLOODBORNE PATHOGEN

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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 4c810d8c-e89b-4e6d-b7c6-c6a079879044
Public Version Date: August 03, 2023
Public Version Number: 6
DI Record Publish Date: September 09, 2016