AquaGuard 50000-SMP

GUDID 10618125192318

AG-SB, SAMPLE KIT

TIDI PRODUCTS, LLC

Cast/bandage waterproof bathing cover, single-use

• Primary Device ID: 10618125192318
• NIH Device Record Key: 2522ae8a-2b6c-46d0-8fe9-9f3e291078f5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AquaGuard
• Version Model Number: 50000-SMP
• Catalog Number: 50000-SMP
• Company DUNS: 063519193
• Company Name: TIDI PRODUCTS, LLC
• 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: true
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	10618125192318 [Primary]

FDA Product Code

• KIA: Cover, Cast

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: 2025-10-01
• Device Publish Date: 2025-09-23

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• 10618125190345: TIDI Moisture Barrier Clear Polyethylene 50 per Box
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• 80618125190313: TIDI Moisture Barrier Clear Polyethylene 98 per Case
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• 80618125190269: TIDI Moisture Barrier Clear Polyethylene 5 per Package
• 80618125190252: TIDI Moisture Barrier Clear Polyethylene 98 per Case
• 10618125192318: AG-SB, SAMPLE KIT