202950

GUDID 10705034000862

SPINAL INSTRUMENT TROCAR

DEPUY SPINE, LLC

Suprapubic catheter introducer, reusable

• Primary Device ID: 10705034000862
• NIH Device Record Key: 3aa5d075-b636-4bb0-bfa0-04e9c616efc6
• Commercial Distribution Discontinuation: 2018-07-31
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: 202950
• Catalog Number: 202950
• Company DUNS: 107105876
• Company Name: DEPUY SPINE, LLC
• 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(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705034000862 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[10705034000862]

Moist Heat or Steam Sterilization

[10705034000862]

Moist Heat or Steam Sterilization

[10705034000862]

Moist Heat or Steam Sterilization

[10705034000862]

Moist Heat or Steam Sterilization

[10705034000862]

Moist Heat or Steam Sterilization

[10705034000862]

Moist Heat or Steam Sterilization

[10705034000862]

Moist Heat or Steam Sterilization

[10705034000862]

Moist Heat or Steam Sterilization

[10705034000862]

Moist Heat or Steam Sterilization

[10705034000862]

Moist Heat or Steam Sterilization

[10705034000862]

Moist Heat or Steam Sterilization

[10705034000862]

Moist Heat or Steam Sterilization

[10705034000862]

Moist Heat or Steam Sterilization

[10705034000862]

Moist Heat or Steam Sterilization

[10705034000862]

Moist Heat or Steam Sterilization

[10705034000862]

Moist Heat or Steam Sterilization

[10705034000862]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2024-02-05
• Device Publish Date: 2016-12-31

Devices Manufactured by DEPUY SPINE, LLC

• 10705034577227 - N/A: 2026-02-10 LATERAL BONE ANCHOR
• 10705034578965 - N/A: 2026-02-10 10° TRIAL 10mm
• 10705034578972 - N/A: 2026-02-10 10° TRIAL 12mm
• 10705034578989 - N/A: 2026-02-10 10° TRIAL 14mm
• 10705034578996 - N/A: 2026-02-10 10° TRIAL 16mm
• 10705034579009 - N/A: 2026-02-10 10° TRIAL 18mm
• 10705034579016 - N/A: 2026-02-10 10° TRIAL 20mm
• 10705034000626 - VSP: 2026-02-09 VSP SPINE SYSTEM ROUND DBL. END IMPACTOR