Patient Barrier Aprons NP3WH

GUDID 10732224004553

Plastic, Waist Length (27 in x 30 in), White

CROSSTEX INTERNATIONAL, INC.

Patient examination/treatment drape, single-use

• Primary Device ID: 10732224004553
• NIH Device Record Key: a36e0d1b-3961-4f35-b6f5-66b288ff5131
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Patient Barrier Aprons
• Version Model Number: NP3WH
• Catalog Number: NP3WH
• Company DUNS: 057728685
• Company Name: CROSSTEX INTERNATIONAL, INC.
• Device Count: 1
• DM Exempt: true
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(585)359-0130
• Email: regulatoryaffairs@hu-friedy.com
• Phone: +1(585)359-0130
• Email: regulatoryaffairs@hu-friedy.com
• Phone: +1(585)359-0130
• Email: regulatoryaffairs@hu-friedy.com
• Phone: +1(585)359-0130
• Email: regulatoryaffairs@hu-friedy.com
• Phone: +1(585)359-0130
• Email: regulatoryaffairs@hu-friedy.com
• Phone: +1(585)359-0130
• Email: regulatoryaffairs@hu-friedy.com
• Phone: +1(585)359-0130
• Email: regulatoryaffairs@hu-friedy.com
• Phone: +1(585)359-0130
• Email: regulatoryaffairs@hu-friedy.com
• Phone: +1(585)359-0130
• Email: regulatoryaffairs@hu-friedy.com
• Phone: +1(585)359-0130
• Email: regulatoryaffairs@hu-friedy.com
• Phone: +1(585)359-0130
• Email: regulatoryaffairs@hu-friedy.com
• Phone: +1(585)359-0130
• Email: regulatoryaffairs@hu-friedy.com
• Phone: +1(585)359-0130
• Email: regulatoryaffairs@hu-friedy.com
• Phone: +1(585)359-0130
• Email: regulatoryaffairs@hu-friedy.com
• Phone: +1(585)359-0130
• Email: regulatoryaffairs@hu-friedy.com
• Phone: +1(585)359-0130
• Email: regulatoryaffairs@hu-friedy.com
• Phone: +1(585)359-0130
• Email: regulatoryaffairs@hu-friedy.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10732224004553 [Primary]

FDA Product Code

• KHR: ABSORBER, SALIVA, PAPER

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: 2023-09-25
• Device Publish Date: 2023-09-15

On-Brand Devices [Patient Barrier Aprons]

• 10732224004638: Nylon, Knee Length (27 in x 44 in), Blue
• 10732224004621: Nylon, Waist Length ( 27 in x 30in), Blue
• 10732224004614: Plastic, Ankle Length (36 in x 54in), White
• 10732224004607: Plastic, Ankle Length (36 in x 54in), Blue
• 10732224004584: Plastic, Knee Length (27 in x 44 in), White
• 10732224004577: Plastic, Knee Length (27 in x 44 in), Blue
• 10732224004553: Plastic, Waist Length (27 in x 30 in), White
• 10732224004546: Plastic, Waist Length (27 in x 30 in), Blue