UnnaCare 4x4 UC4

GUDID 00856525007891

A 4" x4"sterile or non sterile strip or roll of fabric or plastic material (non-natural rubber latex) intended to be applied to and compress a local area of the body for one or more preventative/therapeutic applications (e.g., prevent oedema, support injuries associated with minor trauma, treat disorders of venous return).it is not intended to be used in association with open wounds. It is intended for use in the home or healthcare facility. This is a single-use device.

SUN SCIENTIFIC, INC.

Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use Pressure bandage, non-latex, single-use

• Primary Device ID: 00856525007891
• NIH Device Record Key: 9cc07e54-b88b-4161-bd68-7a9988e6ab66
• Commercial Distribution Discontinuation: 2030-05-18
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: UnnaCare 4x4
• Version Model Number: ZO1050-00
• Catalog Number: UC4
• Company DUNS: 609397224
• Company Name: SUN SCIENTIFIC, INC.
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com
• Phone: 9144795108
• Email: aalward@sun-scientific.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00856525007891 [Primary]

FDA Product Code

• FQM: Bandage, Elastic

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: 2023-03-27
• Device Publish Date: 2023-03-17

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• 00850051939282 - AeroWrap Extension Panel small/medium: 2024-02-06 An extension panel for oversized legs that aids in the extension of the AeroWrap which wraps around the leg and provides compres
• 00850051939299 - AeroWrap Extension Panel Large/XLarge: 2024-02-06 An extension panel for oversized legs that aids in the extension of the AeroWrap which wraps around the leg and provides compres