Express ResultsTM

GUDID 10869419000219

Quest Diagnostics

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• Primary Device ID: 10869419000219
• NIH Device Record Key: b67e23d1-25a2-4e01-8167-04b300fa2a64
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Express ResultsTM
• Version Model Number: UDOA-10CA-0503-01
• Company DUNS: 189222334
• Company Name: Quest Diagnostics
• Device Count: 25
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00869419000212 [Unit of Use]
GS1	10869419000219 [Primary]

FDA Product Code

• LFG: Radioimmunoassay, Tricyclic Antidepressant Drugs

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2021-05-24
• Device Publish Date: 2016-09-24

On-Brand Devices [Express ResultsTM]

• 10869419000240: DOA-154-181
• 10869419000233: UDOA-12CE-0712-01
• 10869419000226: UDOA-10CE-1307-01
• 10869419000219: UDOA-10CA-0503-01
• 10869419000202: UDOA-6CA-0503-01
• 00869419000236: UDOA-12CE-0712-01 (Ox/Cr/pH)++(OXY/PPX)+(mAMP/MOP/PCP)+(BZO/MTD/BAR)+(AMP/COC/THC)MULTI-DRU
• 00869419000243: DOA-154-181(COC/AMP/THC/OPI/PCP)MULTI-DRUG 5 PANEL SCREEN TEST (DOA-154-181) previous (GTIN 1086
• 00869419000212: DUA-1107-061 (Ox/SG/pH)+(mAMP/OPI/PCP)+(BZO/MTD/BAR)+(AMP/COC/THC)+ 5 MULTI-DRUG 10 PANEL U
• 00869419000205: DUA-167-012 (Ox/SG/pH)+(mAMP/OPI/PCP)+(AMP/COC/THC)MULTI-DRUG 6 PANEL INTEGRATED CUP WITH previo