ScanMed Shoulder/Knee (M) Coil

GUDID 00859193006272

SCANMED, LLC

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• Primary Device ID: 00859193006272
• NIH Device Record Key: 5a61e14a-1b76-4aea-b869-746fe13e580e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ScanMed Shoulder/Knee (M) Coil
• Version Model Number: 208GE3001
• Company DUNS: 080151631
• Company Name: SCANMED, 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: false
• 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	00859193006272 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K130457

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: 2017-01-12

On-Brand Devices [ScanMed Shoulder/Knee (M) Coil]

• 00859193006432: 208SI1501
• 00859193006333: 208SI3001
• 00859193006272: 208GE3001
• 00859193006265: 208GE1501