HAND/WRIST COIL N. 3

GUDID 08056304452436

ESAOTE SPA

MRI system coil, radio-frequency

• Primary Device ID: 08056304452436
• NIH Device Record Key: f0b4b789-7e67-47c8-bfc0-b8662cc9ecd9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: HAND/WRIST COIL N. 3
• Version Model Number: 9101912100
• 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	08056304452436 [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

Devices Manufactured by ESAOTE SPA

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• 08056304455062 - 2CWL: 2025-07-15
• 08056304455079 - 5CWL: 2025-07-15
• 08056304455215 - MyLabE85: 2025-07-15
• 08056304455222 - P 1-5E: 2025-07-15
• 08056304455239 - C 1-8E: 2025-07-15
• 08056304455307 - MyLabA70: 2025-07-15
• 08056304455383 - L 3-15E: 2025-07-15