0702034000

GUDID 07613154674930

Fluid Suction HEPA Filter

STRYKER CORPORATION

Surgical fluid/smoke waste management system

• Primary Device ID: 07613154674930
• NIH Device Record Key: 1ece7ace-add1-4e37-a6f1-18c8617a9b7b
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 0702034000
• Catalog Number: 0702034000
• 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: true
• Serial Number: false
• 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	07613154674930 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K132671

FDA Product Code

• JCX: APPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-01-20
• Device Publish Date: 2016-09-23

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