USA Elite System™ and USA Series™ Cold Knife, Serrated Blade

GUDID 00821925002678

Gyrus Acmi, Inc.

Urethrotome

• Primary Device ID: 00821925002678
• NIH Device Record Key: f18be898-e558-4613-89ee-43363af725a3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: USA Elite System™ and USA Series™ Cold Knife, Serrated Blade
• Version Model Number: K-SE
• Company DUNS: 007198742
• Company Name: Gyrus Acmi, Inc.
• 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: 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 Identifiers

Device Issuing Agency	Device ID
GS1	00821925002678 [Package]; Contains: 00821925038417; Package: [3 Units]; In Commercial Distribution
GS1	00821925038417 [Primary]

FDA Product Code

• EZO: Urethrotome

Sterilization

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

[00821925002678]

Ethylene Oxide

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Ethylene Oxide

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Ethylene Oxide

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Ethylene Oxide

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Ethylene Oxide

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Ethylene Oxide

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Ethylene Oxide

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Ethylene Oxide

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Ethylene Oxide

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Ethylene Oxide

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Ethylene Oxide

[00821925002678]

Ethylene Oxide

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Ethylene Oxide

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Ethylene Oxide

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Ethylene Oxide

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Ethylene Oxide

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Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-10-14

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