TxRx CP Extremity Coil

GUDID 00814848020317

QUALITY ELECTRODYNAMICS LLC

MRI system coil, radio-frequency MRI system coil, radio-frequency

• Primary Device ID: 00814848020317
• NIH Device Record Key: 2502a31a-d1da-4cb3-870d-d76614d099df
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TxRx CP Extremity Coil
• Version Model Number: Q7000052
• 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	00814848020317 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K082636

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: 4
• Public Version Date: 2020-03-05
• Device Publish Date: 2016-09-16

On-Brand Devices [TxRx CP Extremity Coil]

• 00814848020317: Q7000052
• 00814848020096: Q7000019