Contour 24

GUDID 00814848020423

QUALITY ELECTRODYNAMICS LLC

MRI system coil, radio-frequency

• Primary Device ID: 00814848020423
• NIH Device Record Key: ed01148d-64aa-4dcb-88b4-85bf16a69dbd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Contour 24
• Version Model Number: Q7000183
• Company DUNS: 614760119
• Company Name: QUALITY ELECTRODYNAMICS LLC
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00814848020423 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K183111

FDA Product Code

• MOS: Coil, Magnetic Resonance, Specialty

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-03-05
• Device Publish Date: 2019-03-21

On-Brand Devices [Contour 24]

• 00814848020256: Q7000184
• 00814848020423: Q7000183