4103-260-000

GUDID 04546540216519

3.25:1 Trinkle

STRYKER CORPORATION

Surgical drill chuck

• Primary Device ID: 04546540216519
• NIH Device Record Key: 6773accf-6265-4663-84f2-ba790c2181ba
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 4103260000
• Catalog Number: 4103-260-000
• Company DUNS: 196548481
• 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: false
• Serial Number: true
• 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)253-3210
• Email: Inst.Stryker.cs@Stryker.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540216519 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K972367

FDA Product Code

• KIJ: INSTRUMENT, SURGICAL, ORTHOPEDIC, DC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

Sterilization

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

[04546540216519]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-01-20
• Device Publish Date: 2018-09-24

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• 07613327662054 - ALPHAVENT: 2025-06-24 ALPHAVENT KNOTLESS SP, 6.5MM, BIOCOMPOSITE ANCHOR