Revital-Ox 2D93Q0

GUDID 00724995094843

Revital-Ox Rigid Container System is for the transport or soaking of rigid endoscopes and accessories.

STERIS CORPORATION

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• Primary Device ID: 00724995094843
• NIH Device Record Key: 7d46361d-f244-4a29-8f74-be69eeccafd8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Revital-Ox
• Version Model Number: 2D93Q0
• Catalog Number: 2D93Q0
• Company DUNS: 139424188
• Company Name: STERIS 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: 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: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
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• Phone: +1(800)548-4873
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• Phone: +1(800)548-4873
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• Phone: +1(800)548-4873
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• Phone: +1(800)548-4873
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• Phone: +1(800)548-4873
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Device Identifiers

Device Issuing Agency	Device ID
GS1	00724995094843 [Primary]

FDA Product Code

• FFY: Adaptor, bulbs, miscellaneous, for endoscope
• PHT: Basin for endoscope reprocessing

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-04-08
• Device Publish Date: 2021-03-31

On-Brand Devices [Revital-Ox]

• 00724995094850: Revital-Ox Flexible Container Round is for the transport or soaking of rigid endoscopes.
• 00724995094843: Revital-Ox Rigid Container System is for the transport or soaking of rigid endoscopes and access