0215-032-000

GUDID 34546540185038

Round Silicone Wound Drain with Trocar

STRYKER CORPORATION

Whole-blood-recovery autotransfusion system, powered

• Primary Device ID: 34546540185038
• NIH Device Record Key: 83da282a-909e-4bb2-9fbc-0432de433b35
• Commercial Distribution Discontinuation: 2019-04-01
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: 0215032000
• Catalog Number: 0215-032-000
• 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 Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540185037 [Primary]
GS1	34546540185038 [Package]; Contains: 04546540185037; Package: pack [10 Units]; Discontinued: 2019-04-01; Not in Commercial Distribution

FDA Product Code

• GCY: APPARATUS, SUCTION, SINGLE PATIENT USE, PORTABLE, NONPOWERED

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: 2020-02-19
• Device Publish Date: 2018-09-24

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