SJM™ 3871

GUDID 05415067023810

Patient Controller App

ADVANCED NEUROMODULATION SYSTEMS, INC.

Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer

• Primary Device ID: 05415067023810
• NIH Device Record Key: 156d29e1-8364-4f48-a62e-27fd032ca898
• Commercial Distribution Discontinuation: 2018-03-28
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: SJM™
• Version Model Number: 3871
• Catalog Number: 3871
• Company DUNS: 021675699
• Company Name: ADVANCED NEUROMODULATION SYSTEMS, INC.
• 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: 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(855)478-5833
• Email: customerservice@sjm.com
• Phone: +1(855)478-5833
• Email: customerservice@sjm.com
• Phone: +1(855)478-5833
• Email: customerservice@sjm.com
• Phone: +1(855)478-5833
• Email: customerservice@sjm.com
• Phone: +1(855)478-5833
• Email: customerservice@sjm.com
• Phone: +1(855)478-5833
• Email: customerservice@sjm.com
• Phone: +1(855)478-5833
• Email: customerservice@sjm.com
• Phone: +1(855)478-5833
• Email: customerservice@sjm.com
• Phone: +1(855)478-5833
• Email: customerservice@sjm.com
• Phone: +1(855)478-5833
• Email: customerservice@sjm.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	05415067023810 [Primary]

FDA Product Code

• LGW: STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2018-10-22
• Device Publish Date: 2015-07-30

On-Brand Devices [SJM™]

• 05415067023810: Patient Controller App
• 05415067023803: Clinician Programmer App
• 05414734402477: 3701
• 05414734401005: 1291
• 05414734400985: 1280
• 05414734400794: Communication Wand
• 05414734400763: 1210
• 15414734400173: 1120
• 15414734400135: Epidural Needle, 15 gauge, 4" (10cm)
• 15414734400104: 1112
• 15414734400012: 1101