DRI Ethyl Alcohol Assay

GUDID 00884883002890

Microgenics Corporation

Ethanol (ETOH) IVD, kit, enzyme spectrophotometry

• Primary Device ID: 00884883002890
• NIH Device Record Key: 7e56203f-ff7c-42e2-8dd9-221a3ef0e912
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DRI Ethyl Alcohol Assay
• Version Model Number: 0038
• Company DUNS: 122153799
• Company Name: Microgenics Corporation
• Device Count: 1
• 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	00884883002890 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K923783

FDA Product Code

• DMT: Enzymatic Method, Alcohol Dehydrogenase, Ultraviolet

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: 2018-07-06
• Device Publish Date: 2016-09-12

On-Brand Devices [DRI Ethyl Alcohol Assay]

• 00884883012486: 10016397
• 00884883002890: 0038
• 00884883001008: 0037