MediDrapes Inc.

GUDID 00618125160914

MediDrapes Inc. C-arm Equipment Covers Clear Polyethylene Sterile Fits OEC 9600/9800, Siemens ARCADIS Avantic, Sieme 20 per Case

TIDI PRODUCTS, LLC

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• Primary Device ID: 00618125160914
• NIH Device Record Key: 41800039-15ad-422d-aeca-38369ed3ea22
• Commercial Distribution Discontinuation: 2023-02-28
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: MediDrapes Inc.
• Version Model Number: 30554
• 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	00618125160914 [Package]; Contains: 01618125160913; Package: [20 Units]; Discontinued: 2023-02-28; Not in Commercial Distribution
GS1	01618125160913 [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: 3
• Public Version Date: 2023-03-01
• Device Publish Date: 2016-10-12

On-Brand Devices [MediDrapes Inc.]

• 00618125160914: MediDrapes Inc. C-arm Equipment Covers Clear Polyethylene Sterile Fits OEC 9600/9800, Siemens AR
• 00618125163977: MediDrapes Inc. C-arm Equipment Covers Clear Polyethylene Sterile 54in x 60in x 1in 40 per Case