AccessGUDID - DEVICE: Dimension® Flex® reagent cartridge THC (00842768005855)

GUDID

Device Identifier (DI) Information

Brand Name: Dimension® Flex® reagent cartridge THC
Version or Model: 10444925
Commercial Distribution Status: In Commercial Distribution
Catalog Number: DF95A
Company Name: Siemens Healthcare Diagnostics Inc.

Primary DI Number: 00842768005855
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 4
Labeler D-U-N-S® Number*: 005088112 *Terms of Use

Device Description: Urine Cannabinoids Screen Flex® reagent cartridge, 80 tests

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:	No
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?
55550	Cannabinoid/cannabinoid metabolite IVD, kit, enzyme immunoassay (EIA)	A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of cannabinoids and/or cannabinoid metabolites (i.e., natural, synthetic) in a clinical specimen, using an enzyme immunoassay (EIA) method.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LDJ	ENZYME IMMUNOASSAY, CANNABINOIDS

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K000461	000

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
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: 2dffae9d-b125-4ec0-a0d6-d732e7a73079
Public Version Date: November 28, 2022
Public Version Number: 6
DI Record Publish Date: September 24, 2016