General SR0117

GUDID 10889981140267

Locking Driver, Free Sleeve

SEASPINE ORTHOPEDICS CORPORATION

Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver Orthopaedic implant driver

• Primary Device ID: 10889981140267
• NIH Device Record Key: 8bc09df1-6f0a-40d9-8e4e-2a2840db6803
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: General
• Version Model Number: SR0117
• Catalog Number: SR0117
• Company DUNS: 079840876
• Company Name: SEASPINE ORTHOPEDICS CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com
• Phone: +1(760)727-8399
• Email: custsvcspine@seaspine.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10889981140267 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[10889981140267]

Moist Heat or Steam Sterilization

[10889981140267]

Moist Heat or Steam Sterilization

[10889981140267]

Moist Heat or Steam Sterilization

[10889981140267]

Moist Heat or Steam Sterilization

[10889981140267]

Moist Heat or Steam Sterilization

[10889981140267]

Moist Heat or Steam Sterilization

[10889981140267]

Moist Heat or Steam Sterilization

[10889981140267]

Moist Heat or Steam Sterilization

[10889981140267]

Moist Heat or Steam Sterilization

[10889981140267]

Moist Heat or Steam Sterilization

[10889981140267]

Moist Heat or Steam Sterilization

[10889981140267]

Moist Heat or Steam Sterilization

[10889981140267]

Moist Heat or Steam Sterilization

[10889981140267]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-10-02
• Device Publish Date: 2020-09-24

On-Brand Devices [General]

• 10889981144296: Palm Style Probe
• 10889981144265: 3.5mm Tap File
• 10889981143497: Dilator 5 Threaded File
• 10889981140267: Locking Driver, Free Sleeve
• 10889981159474: TruProfile Plate Caddy
• 10889981143343: Slap Hammer, 3/8 Male
• 10889981289362: Suction Tip, #10
• 10889981289355: Suction Tip, #8
• 10889981286934: Alpha Universal Lid, 20 X 10