01-02970

GUDID 04546540134578

ARCH BAR, WINTER

Stryker Leibinger GmbH & Co. KG

Orthopaedic surgical procedure kit, non-medicated, single-use

• Primary Device ID: 04546540134578
• NIH Device Record Key: f83b3487-4cb6-44da-b28f-e6adf0741266
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 01-02970
• Catalog Number: 01-02970
• Company DUNS: 316153956
• Company Name: Stryker Leibinger GmbH & Co. KG
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Length: 14 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540134578 [Primary]

FDA Product Code

• EHO: BAR, PREFORMED

Sterilization

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

[04546540134578]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-30

Devices Manufactured by Stryker Leibinger GmbH & Co. KG

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