AccessGUDID - DEVICE: Origin Instant Oral Drug Test (B77881025ODEI0)

GUDID

Device Identifier (DI) Information

Brand Name: Origin Instant Oral Drug Test
Version or Model: 81025-OD-EI
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 81025-OD-EI
Company Name: ORIGIN DIAGNOSTICS LLC

Primary DI Number: B77881025ODEI0
Issuing Agency: HIBCC
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 036225773 *Terms of Use

Device Description: Origin Instant Oral Drug Test, AMP-BAR-BUP-BZO-COC-MDMA-MET-OPI-OXY-THC

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

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GMDN Names and Definitions: © Copyright GMDN Agency 2015. Reproduced with Permission from the GMDN Agency.

GMDN Preferred Term Name	GMDN Definition
Multiple drugs of abuse IVD, kit, immunochromatographic test (ICT), rapid	A collection of reagents and other associated materials intended to be used for the qualitative and/or semi-quantitative detection of multiple drugs of abuse in a clinical specimen within a short period, relative to standard laboratory testing procedures, using an immunochromatographic test (ICT) method. This test is commonly used in the laboratory or in point-of-care analyses. It is not intended to be used for self-testing.

GMDN Preferred Term Name

GMDN Definition

Multiple drugs of abuse IVD, kit, immunochromatographic test (ICT), rapid

A collection of reagents and other associated materials intended to be used for the qualitative and/or semi-quantitative detection of multiple drugs of abuse in a clinical specimen within a short period, relative to standard laboratory testing procedures, using an immunochromatographic test (ICT) method. This test is commonly used in the laboratory or in point-of-care analyses. It is not intended to be used for self-testing.

FDA Product Code

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Product Code	Product Code Name
PVJ	Test, Cannabinoid, Employment And Insurance Testing, Exempt
PVD	Test, Methamphetamine, Employment And Insurance Testing, Exempt
PVA	Test, Cocaine And Cocaine Metabolite, Employment And Insurance Testing, Exempt
PUZ	Test, Benzodiazepine, Employment And Insurance Testing, Exempt
PVH	Test, Opiates, Employment And Insurance Testing, Exempt
PUY	Test, Barbiturate, Employment And Insurance Testing, Exempt
PUX	Test, Amphetamine, Employment And Insurance Testing, Exempt

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 30 Degrees Celsius

Clinically Relevant Size

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Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 70947f7f-4beb-4efc-b706-6887c4ccaa84
Public Version Date: May 24, 2021
Public Version Number: 2
DI Record Publish Date: January 24, 2020