Connection cable

GUDID 18054655000402

SPES MEDICA SRL

Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead Analytical non-scalp cutaneous lead

• Primary Device ID: 18054655000402
• NIH Device Record Key: 8f4c8109-c054-4255-8e64-e4798a997d47
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Connection cable
• Version Model Number: 2001PUD7126SH
• Company DUNS: 514029771
• Company Name: SPES MEDICA SRL
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	18054655000402 [Primary]

FDA Product Code

• IKD: Cable, Electrode

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-12-30
• Device Publish Date: 2021-12-22

Devices Manufactured by SPES MEDICA SRL

• 18054655026815 - Recording and stimulating for Central Nervous System electrodes: 2022-12-07
• 18054655028222 - Recording and stimulating for Central Nervous System electrodes: 2022-12-07
• 18054655028239 - Recording and stimulating for Central Nervous System electrodes: 2022-12-07
• 18054655000402 - Connection cable: 2021-12-30
• 18054655000402 - Connection cable: 2021-12-30
• 08054655023664 - AC Cream - Conductive Paste: 2021-12-30
• 08054655031843 - SafePrep: 2021-08-13
• 18054655025979 - Urethral Catheter Electrode: 2021-06-01
• 18054655026013 - Urethral Catheter Electrode: 2021-06-01