DISCOVERY 275726000

GUDID 10705034300290

DISCOVERY SCREW SYSTEM OBTURATOR

DEPUY SPINE, LLC

Surgical drill guide obturator

• Primary Device ID: 10705034300290
• NIH Device Record Key: d08f1322-6c69-47de-8f21-8353a44b9581
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DISCOVERY
• Version Model Number: 275726000
• Catalog Number: 275726000
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705034300290 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[10705034300290]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-04-15
• Device Publish Date: 2019-04-05

On-Brand Devices [DISCOVERY]

• 10705034300290: DISCOVERY SCREW SYSTEM OBTURATOR
• 10705034034614: DISCOVERY SCREW SYSTEM WASHER