O.I.C. TITANIUM 873011

GUDID 07613327261899

DURA MATER RETRACTOR

Stryker Corporation

Nerve/vessel retractor

• Primary Device ID: 07613327261899
• NIH Device Record Key: 8fa81966-2465-466d-85d8-52e12b2b5780
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: O.I.C. TITANIUM
• Version Model Number: 873011
• Catalog Number: 873011
• Company DUNS: 149183167
• Company Name: Stryker 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327261899 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[07613327261899]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-11-18
• Device Publish Date: 2019-11-08

On-Brand Devices [O.I.C. TITANIUM]

• 07613327261981: REAMER
• 07613327261936: REAMER
• 07613327261912: REAMER
• 07613327261905: REAMER
• 07613327261851: REAMER
• 07613327261837: REAMER
• 07613327261899: DURA MATER RETRACTOR
• 07613327261875: ROOT RETRACTOR
• 07613327261790: INSTRUMENT TRAY
• 07613327261783: IMPLANT TRAY CONTAINER
• 07613327261813: CAGE SUPPORT
• 07613327261806: BONE GRAFT IMPACTOR
• 07613327261882: DISTRACTOR