MixEvac 0206015000

GUDID 34546540447792

3 Bone Cement Mixer

STRYKER CORPORATION

Manual orthopaedic cement mixer, reusable

• Primary Device ID: 34546540447792
• NIH Device Record Key: a8a38d5c-2c95-4fe1-b37b-d42ca5488e14
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MixEvac
• Version Model Number: 0206015000
• Catalog Number: 0206015000
• Company DUNS: 196548481
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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	04546540447791 [Primary]
GS1	34546540447792 [Package]; Contains: 04546540447791; Package: pack [10 Units]; In Commercial Distribution

FDA Product Code

• JDZ: MIXER, CEMENT, FOR CLINICAL USE

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-10-25
• Device Publish Date: 2018-09-24

On-Brand Devices [MixEvac]

• 37613154358336: 3 Bone Cement Mixer with Small Spatula
• 34546540447792: 3 Bone Cement Mixer