VV-PLUG VV-PLUG

GUDID 00802526497544

Oscor Inc.

Cardiac pulse generator port plug

• Primary Device ID: 00802526497544
• NIH Device Record Key: b43451de-218f-4c30-8ef5-7fca7d27b725
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VV-PLUG
• Version Model Number: 667145-301
• Catalog Number: VV-PLUG
• Company DUNS: 101835833
• Company Name: Oscor 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00802526497544 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K031164

FDA Product Code

• DTB: Permanent Pacemaker Electrode

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: 2016-07-07

On-Brand Devices [VV-PLUG]

• 00802526540608: 667145-750
• 00802526497544: 667145-301
• 00885672008307: 667145-751
• 00885672008291: 667145-302
• 00836559002857: VV-PLUG