AO 4100-210-000S1

GUDID 07613154055180

Large Reamer

STRYKER CORPORATION

Surgical drill chuck

• Primary Device ID: 07613154055180
• NIH Device Record Key: eec6a7a6-f5df-467e-9614-957cd30627f0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AO
• Version Model Number: 4100210000S1
• Catalog Number: 4100-210-000S1
• 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
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613154055180 [Primary]

FDA Product Code

• HRX: ARTHROSCOPE

Sterilization

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

[07613154055180]

Moist Heat or Steam Sterilization

[07613154055180]

Moist Heat or Steam Sterilization

[07613154055180]

Moist Heat or Steam Sterilization

[07613154055180]

Moist Heat or Steam Sterilization

[07613154055180]

Moist Heat or Steam Sterilization

[07613154055180]

Moist Heat or Steam Sterilization

[07613154055180]

Moist Heat or Steam Sterilization

[07613154055180]

Moist Heat or Steam Sterilization

[07613154055180]

Moist Heat or Steam Sterilization

[07613154055180]

Moist Heat or Steam Sterilization

[07613154055180]

Moist Heat or Steam Sterilization

[07613154055180]

Moist Heat or Steam Sterilization

[07613154055180]

Moist Heat or Steam Sterilization

[07613154055180]

Moist Heat or Steam Sterilization

[07613154055180]

Moist Heat or Steam Sterilization

[07613154055180]

Moist Heat or Steam Sterilization

[07613154055180]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 8
• Public Version Date: 2019-11-22
• Device Publish Date: 2017-02-23

On-Brand Devices [AO]

• 07613327115123: Right Angle Drive - Large Reamer
• 07613154055180: Large Reamer
• 04546540501707: Large Reamer
• 04546540501615: Small Drill
• 04546540216472: 3.25:1 Large Reamer
• 04546540216403: 1:1 Small Drill
• 04546540068217: Large Reamer
• 04546540068156: Small Drill