LUMBAR COIL N. 17

GUDID 08056304452368

Coil for S-scan

ESAOTE SPA

MRI system coil, radio-frequency

• Primary Device ID: 08056304452368
• NIH Device Record Key: 353b6f87-3360-4d40-95ca-8d82d419d675
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LUMBAR COIL N. 17
• Version Model Number: 131000200
• Company DUNS: 437384304
• Company Name: ESAOTE SPA
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08056304452368 [Primary]

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: 3
• Public Version Date: 2020-03-05
• Device Publish Date: 2016-09-27

On-Brand Devices [LUMBAR COIL N. 17 ]

• 08056304452894: Coil for G-scan
• 08056304452382: Coil for G-scan Brio
• 08056304452368: Coil for S-scan