Fog Guard Anti-Fog Solution with Sponge

GUDID 20787551000003

XODUS MEDICAL, INC.

Endoscopic antifog solution Endoscopic antifog solution

• Primary Device ID: 20787551000003
• NIH Device Record Key: d7f81a12-a9d8-430a-94be-2041fa7726fe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fog Guard Anti-Fog Solution with Sponge
• Version Model Number: 30900
• Company DUNS: 868042664
• Company Name: XODUS MEDICAL, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00787551000009 [Primary]
GS1	20787551000003 [Package]; Contains: 00787551000009; Package: [20 Units]; In Commercial Distribution

FDA Product Code

• OCT: Anti fog solution and accessories, endoscopy

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-03-28

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