Zonare

GUDID 01618125168162

Zonare Clear Polyethylene Sterile 36in x 22in x 1in 25 per Case

TIDI PRODUCTS, LLC

Medical equipment drape, single-use

• Primary Device ID: 01618125168162
• NIH Device Record Key: 05408758-1361-42f5-8604-28c19eb3598b
• Commercial Distribution Discontinuation: 2022-09-22
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Zonare
• Version Model Number: 29187
• 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: false
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	01618125168162 [Primary]

FDA Product Code

• KKX: Drape, surgical

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2024-07-25
• Device Publish Date: 2016-10-12

On-Brand Devices [Zonare]

• 10618125168160: Zonare Clear Polyethylene Sterile 36in x 22in x 1in 25 per Case
• 01618125168162: Zonare Clear Polyethylene Sterile 36in x 22in x 1in 25 per Case