92-07761

GUDID 07613327504491

L-PLATE, RIGHT, GSP

Stryker Leibinger GmbH & Co. KG

Craniofacial fixation plate, non-bioabsorbable

• Primary Device ID: 07613327504491
• NIH Device Record Key: 59798948-6e3c-4578-8e68-d0145010e79a
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 92-07761
• Catalog Number: 92-07761
• Company DUNS: 316153956
• Company Name: Stryker Leibinger GmbH & Co. KG
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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

• Device Size Text, specify: 0
• Angle: 100 degree
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Angle: 100 degree
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Angle: 100 degree
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Angle: 100 degree
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Angle: 100 degree
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Angle: 100 degree
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Angle: 100 degree
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Angle: 100 degree
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Angle: 100 degree
• Device Size Text, specify: 0
• Device Size Text, specify: 0
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• Device Size Text, specify: 0
• Device Size Text, specify: 0
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• Device Size Text, specify: 0
• Device Size Text, specify: 0
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• Device Size Text, specify: 0
• Device Size Text, specify: 0
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• Device Size Text, specify: 0
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• Device Size Text, specify: 0
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• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Angle: 100 degree
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Angle: 100 degree
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Angle: 100 degree
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Angle: 100 degree
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Angle: 100 degree
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Angle: 100 degree
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Angle: 100 degree
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327504491 [Primary]

FDA Product Code

• JEY: PLATE, BONE

Sterilization

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

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

[07613327504491]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2021-02-05
• Device Publish Date: 2019-10-10

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