CEDIA Propoxyphene Assay

GUDID 00884883004221

Microgenics Corporation

Propoxyphene IVD, kit, enzyme immunoassay (EIA)

• Primary Device ID: 00884883004221
• NIH Device Record Key: cd8f3c17-14b6-4b4a-8e65-5d75ef207cd5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CEDIA Propoxyphene Assay
• Version Model Number: 100170
• 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	00884883004221 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K951133

FDA Product Code

• JXN: Enzyme Immunoassay, Propoxyphene

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 [CEDIA Propoxyphene Assay]

• 00884883004283: 100171
• 00884883004221: 100170