CEDIA Multi-Drug Intermediate Calibrator

GUDID 00884883002050

Microgenics Corporation

Multiple drugs of abuse IVD, calibrator

• Primary Device ID: 00884883002050
• NIH Device Record Key: 16b7a4e3-eed3-4897-9b68-e5e3e5d5806e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CEDIA Multi-Drug Intermediate Calibrator
• Version Model Number: 1732218
• Company DUNS: 122153799
• Company Name: Microgenics Corporation
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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	00884883002050 [Primary]

FDA Product Code

• DKB: Calibrators, Drug Mixture

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: 2019-07-04
• Device Publish Date: 2016-09-24

On-Brand Devices [CEDIA Multi-Drug Intermediate Calibrator]

• 00884883002050: 1732218
• 00884883002005: 1730380