GUDID 20613994802501

PROBE PSP1001 10PK 175MM PEDI SCREW ROHS

MEDTRONIC XOMED, INC.

Nerve-locating system, line-powered

• Primary Device ID: 20613994802501
• NIH Device Record Key: 827f13b1-5c7e-4d2e-bfda-510e28ef1fc0
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: PSP1001
• Company DUNS: 835465063
• Company Name: MEDTRONIC XOMED, 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: true
• 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(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Dimensions

• Length: 175 Millimeter
• Length: 175 Millimeter
• Length: 175 Millimeter
• Length: 175 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00613994802507 [Primary]
GS1	20613994802501 [Package]; Contains: 00613994802507; Package: PK [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K062996

FDA Product Code

• GXZ: ELECTRODE, NEEDLE

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: 2016-04-30

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