Urocare® Adhesive Remover Pads (Box of 50) 5600

GUDID 00792293056009

ADHESIVE REMOVER, PADS, WIPES, SACHETTE, SILICONE, URINE COLLECTION, OSTOMY, MALE EXTERNAL CATHETER, LATEX-FREE, NON-FLAMMABLE Urocare® adhesive remover has been specifically formulated for dissolving and removing unwanted adhesive or adhesive residue from urinary and ostomy appliances, tens units, monitoring electrodes, skin and can even be used for the removal of tar. Packaged in a small, convenient wipe, Urocare® adhesive remover pads are the perfect solution to aid in the removal of adhesive residue left behind by male external catheters. They may be used to soften the adhesive of double-sided adhesive foam strips as well as most brush-on medical adhesives. They contain a lab tested, non-toxic, citrus-based solution that may also be used to remove these types of medical adhesives or adhesive residue from skin and appliances in preparation for the use of a new adhesive strip/wafer. It is recommended that a male external catheter be changed once a day to promote healthy skin. With the use of Urocare® adhesive remover pads, a male external catheter can be changed quickly and easily. Key Features: • NON-TOXIC—Lab Tested, non-toxic and free from harsh solvents. • Citrus-Based—Fresh citrus scent and biodegradable. • Many Uses—Use on nitro patches, tens units, electrodes, even tar. • Convenient—Travel size pads are small and easy to use • Soap & Water Clean-Up—Just wash, rinse and dry • Suitable for Hospital, Long-Term Care and Home Use • Alcohol-Free Formula • Environmentally Friendly—Does not contain ozone-depleting chloro-fluorocarbons • Convenient Packaging—Use only what you need so there's less waste Note: For external use only.

UROCARE PRODUCTS, INC.

Patient medical adhesive remover

• Primary Device ID: 00792293056009
• NIH Device Record Key: 45bbbb89-9244-4af1-8125-1fa0572542a7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Urocare® Adhesive Remover Pads (Box of 50)
• Version Model Number: 5600
• Catalog Number: 5600
• Company DUNS: 070637129
• Company Name: UROCARE PRODUCTS, 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: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 909-621-6013
• Email: CUST.SUPPORT@UROCARE.COM
• Phone: 909-621-6013
• Email: CUST.SUPPORT@UROCARE.COM
• Phone: 909-621-6013
• Email: CUST.SUPPORT@UROCARE.COM
• Phone: 909-621-6013
• Email: CUST.SUPPORT@UROCARE.COM
• Phone: 909-621-6013
• Email: CUST.SUPPORT@UROCARE.COM
• Phone: 909-621-6013
• Email: CUST.SUPPORT@UROCARE.COM
• Phone: 909-621-6013
• Email: CUST.SUPPORT@UROCARE.COM
• Phone: 909-621-6013
• Email: CUST.SUPPORT@UROCARE.COM
• Phone: 909-621-6013
• Email: CUST.SUPPORT@UROCARE.COM

Device Dimensions

• Weight: 0.004 Pound
• Weight: 0.004 Pound
• Weight: 0.004 Pound
• Weight: 0.004 Pound
• Weight: 0.004 Pound
• Weight: 0.004 Pound
• Weight: 0.004 Pound
• Weight: 0.004 Pound
• Width: 2.25 Inch
• Depth: 0.1 Inch
• Height: 2.25 Inch
• Weight: 0.004 Pound
• Width: 2.25 Inch
• Depth: 0.1 Inch
• Height: 2.25 Inch
• Weight: 0.004 Pound
• Width: 2.25 Inch
• Depth: 0.1 Inch
• Height: 2.25 Inch
• Weight: 0.004 Pound
• Width: 2.25 Inch
• Depth: 0.1 Inch
• Height: 2.25 Inch
• Weight: 0.004 Pound
• Width: 2.25 Inch
• Depth: 0.1 Inch
• Height: 2.25 Inch
• Weight: 0.004 Pound
• Width: 2.25 Inch
• Depth: 0.1 Inch
• Height: 2.25 Inch
• Weight: 0.004 Pound

Device Identifiers

Device Issuing Agency	Device ID
GS1	00792293056009 [Primary]

FDA Product Code

• KOX: Solvent, Adhesive Tape

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-03-11
• Device Publish Date: 2018-06-01

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