3D Offset Imaging Set SPX1

GUDID 03701311500971

ECENTIAL ROBOTICS

Imaging lesion localization marker, external, single-use

• Primary Device ID: 03701311500971
• NIH Device Record Key: 18bb7408-e22b-4a5b-91c9-2c5931b6334b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 3D Offset Imaging Set SPX1
• Version Model Number: A01038
• Company DUNS: 261610964
• Company Name: ECENTIAL ROBOTICS
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +33458005520
• Email: service@ecential-robotics.com
• Phone: +33458005520
• Email: service@ecential-robotics.com
• Phone: +33458005520
• Email: service@ecential-robotics.com
• Phone: +33458005520
• Email: service@ecential-robotics.com
• Phone: +33458005520
• Email: service@ecential-robotics.com
• Phone: +33458005520
• Email: service@ecential-robotics.com
• Phone: +33458005520
• Email: service@ecential-robotics.com
• Phone: +33458005520
• Email: service@ecential-robotics.com
• Phone: +33458005520
• Email: service@ecential-robotics.com
• Phone: +33458005520
• Email: service@ecential-robotics.com
• Phone: +33458005520
• Email: service@ecential-robotics.com
• Phone: +33458005520
• Email: service@ecential-robotics.com
• Phone: +33458005520
• Email: service@ecential-robotics.com
• Phone: +33458005520
• Email: service@ecential-robotics.com
• Phone: +33458005520
• Email: service@ecential-robotics.com
• Phone: +33458005520
• Email: service@ecential-robotics.com
• Phone: +33458005520
• Email: service@ecential-robotics.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	03701311500971 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K220946

FDA Product Code

• OWB: Interventional Fluoroscopic X-Ray System

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-09-12
• Device Publish Date: 2023-09-04

On-Brand Devices [3D Offset Imaging Set SPX1]

• 03701311500391: A00038
• 03701311500971: A01038