Nevro® MADP2008-25B

GUDID 00813426020107

Blue M8 Lead Adaptor Kit, 25cm

NEVRO CORP.

Neural-tissue electrical stimulation lead adaptor

• Primary Device ID: 00813426020107
• NIH Device Record Key: e8c92dbf-7f5a-46a5-bacb-1fc693696c1e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nevro®
• Version Model Number: MADP2008-25B
• Catalog Number: MADP2008-25B
• Company DUNS: 926599155
• Company Name: NEVRO CORP.
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 6502510005
• Email: info@nevro.com
• Phone: 6502510005
• Email: info@nevro.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813426020107 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P130022

FDA Product Code

• LGW: Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-05-21

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