NAVIGATED MANTIS 48769210

GUDID 07613327065190

T-HANDLE RATCHET

Stryker Corporation

Surgical instrument handle, non-torque-limiting

• Primary Device ID: 07613327065190
• NIH Device Record Key: 38f1afda-48f6-44a1-81dd-d316d225138b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NAVIGATED MANTIS
• Version Model Number: 48769210
• Catalog Number: 48769210
• Company DUNS: 149183167
• Company Name: Stryker Corporation
• Device Count: 1
• 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: 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	07613327065190 [Primary]

FDA Product Code

• OLO: Orthopedic stereotaxic instrument

Sterilization

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

[07613327065190]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-11-22
• Device Publish Date: 2016-09-24

On-Brand Devices [NAVIGATED MANTIS]

• 07613327121537: TRAY
• 07613327065190: T-HANDLE RATCHET
• 07613327065183: POLYAXIAL SCREWDRIVER
• 07613327065176: CANNULATED AWL
• 07613327065169: POLYAXIAL SCREWDRIVER
• 07613327065152: TAP SLEEVE
• 07613327065145: CANNULATED TAP
• 07613327065138: CANNULATED TAP
• 07613327065121: CANNULATED TAP
• 07613327065114: CANNULATED TAP
• 07613327065107: CANNULATED TAP