ScanMed PROCURE™ Coil

GUDID 00859193006449

SCANMED, LLC

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• Primary Device ID: 00859193006449
• NIH Device Record Key: d31968d2-df4d-4e0a-a1e9-cd2fda75925d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ScanMed PROCURE™ Coil
• Version Model Number: 508PH1501
• 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	00859193006449 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K140606

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: 2017-11-10

On-Brand Devices [ScanMed PROCURE™ Coil]

• 00859193006456: 508PH3001
• 00859193006449: 508PH1501
• 00859193006425: 588PH3001
• 00859193006371: 588PH1501
• 00859193006210: 588SI1501
• 00859193006203: 588GE3001
• 00859193006197: 588GE1501
• 00859193006142: 508SI3001
• 00859193006135: 508SI1501
• 00859193006128: 508GE3001
• 00859193006111: 508GE1501
• 00859193006005: 588SI3001