LIGATURE SLEEVE LS21-10

GUDID 20802526563229

Oscor Inc.

Endocardial defibrillation lead

• Primary Device ID: 20802526563229
• NIH Device Record Key: 47f2065c-3626-4b57-b74a-64601447109d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LIGATURE SLEEVE
• Version Model Number: 664760-302
• Catalog Number: LS21-10
• Company DUNS: 101835833
• Company Name: Oscor Inc.
• Device Count: 10
• 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	00802526563225 [Unit of Use]
GS1	20802526563229 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K020669

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 [LIGATURE SLEEVE]

• 70836559007424: LS17B20
• 70836559002023: LS26B20
• 70836559002016: LS24B20
• 70836559002009: LS21B20
• 70836559001996: LS18B20
• 70836559001989: LS15B20
• 20885672008349: Ligature Sleeve
• 20802526563229: 664760-302
• 00836559007425: LS-17
• 00836559002024: LS-26
• 00836559002017: LS-24
• 00836559002000: LS-21
• 00836559001997: LS-18
• 00836559001980: LS-15