Howmedica, Definition 6265004311

GUDID 07613327116618

Femoral Pressuring Seal Size 4-7

STRYKER CORPORATION

Orthopaedic cement/bone filler dispensing gun Orthopaedic cement/bone filler dispensing gun Orthopaedic cement/bone filler dispensing gun Orthopaedic cement/bone filler dispensing gun Orthopaedic cement/bone filler dispensing gun Orthopaedic cement/bone filler dispensing gun Orthopaedic cement/bone filler dispensing gun Orthopaedic cement/bone filler dispensing gun Orthopaedic cement/bone filler dispensing gun Orthopaedic cement/bone filler dispensing gun

• Primary Device ID: 07613327116618
• NIH Device Record Key: 50e08358-ae0a-46da-8cd1-87d4e83ad835
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Howmedica, Definition
• Version Model Number: 6265004311
• Catalog Number: 6265004311
• 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
• 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

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store in Cool Dry Place
• Special Storage Condition, Specify: Between 0 and 0 *Store in Cool Dry Place
• Special Storage Condition, Specify: Between 0 and 0 *Store in Cool Dry Place
• Special Storage Condition, Specify: Between 0 and 0 *Store in Cool Dry Place
• Special Storage Condition, Specify: Between 0 and 0 *Store in Cool Dry Place
• Special Storage Condition, Specify: Between 0 and 0 *Store in Cool Dry Place
• Special Storage Condition, Specify: Between 0 and 0 *Store in Cool Dry Place
• Special Storage Condition, Specify: Between 0 and 0 *Store in Cool Dry Place
• Special Storage Condition, Specify: Between 0 and 0 *Store in Cool Dry Place
• Special Storage Condition, Specify: Between 0 and 0 *Store in Cool Dry Place

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327116618 [Primary]

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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-02-07
• Device Publish Date: 2018-09-24

On-Brand Devices [Howmedica, Definition]

• 07613327116618: Femoral Pressuring Seal Size 4-7
• 04546540263179: Femoral Pressuring Seal Size 1-4