AccessGUDID - DEVICE: Preknow THC (Marijuana) Single Drug Screen Test (15 Dipcards) (00857275007124)

GUDID

Device Identifier (DI) Information

Brand Name: Preknow THC (Marijuana) Single Drug Screen Test (15 Dipcards)
Version or Model: IDTH-115-15P
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: IDUN SOLUTIONS LLC

Primary DI Number: 00857275007124
Issuing Agency: GS1
Commercial Distribution End Date: January 01, 2022
Device Count: 1
Labeler D-U-N-S® Number*: 080651010 *Terms of Use

Device Description: 15 THC test dip-cards

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):	Yes
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?
30519	Cannabinoid/cannabinoid metabolite IVD, kit, rapid ICT, clinical	A collection of reagents and other associated materials intended to be used for the qualitative and/or (semi-)quantitative detection of cannabinoids and/or cannabinoid metabolites (i.e., natural, synthetic) in a clinical specimen within a short period, relative to standard laboratory testing procedures, using an immunochromatographic test (ICT) method [lateral flow test]. This is a rapid test used in the laboratory or in point-of-care analyses. It is not intended to be used for self-testing.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
LDJ	Enzyme Immunoassay, Cannabinoids

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K153050	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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 9de048b1-35b6-4b2e-b660-2c643c2b0fb9
Public Version Date: November 28, 2022
Public Version Number: 7
DI Record Publish Date: May 16, 2017