Connection cable

GUDID 08054655021707

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

• Primary Device ID: 08054655021707
• NIH Device Record Key: 483a9c8c-68dc-4ce9-b97b-0fb24c6dcc52
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Connection cable
• Version Model Number: SBM1AE002
• Company DUNS: 514029771
• Company Name: SPES MEDICA SRL
• Device Count: 2
• 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: true
• 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	08054655021707 [Unit of Use]
GS1	18054655021704 [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: 2024-05-21
• Device Publish Date: 2024-05-13

On-Brand Devices [Connection cable]

• 18054655000402: 2001PUD7126SH
• 08054655030037: SBM1AE004
• 08054655021714: SBM1AE003
• 08054655021707: SBM1AE002
• 08054655020793: SBM1AE001