Pocket Press

GUDID 10860280002609

Post-CIED Implant Compression Bandage

COMPRESS INNOVATIONS, LLC

Pressure bandage, non-latex, single-use

• Primary Device ID: 10860280002609
• NIH Device Record Key: 9b4d7dcf-a9b5-4373-afe3-7209ec7609b7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pocket Press
• Version Model Number: PKT21
• Company DUNS: 035534207
• Company Name: COMPRESS INNOVATIONS, LLC
• Device Count: 3
• 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: true
• Manufacturing Date: false
• 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: false

Customer Support Contacts

• Phone: 929-444-9115
• Email: customerservice@compressinnovations.com
• Phone: 929-444-9115
• Email: customerservice@compressinnovations.com
• Phone: 929-444-9115
• Email: customerservice@compressinnovations.com
• Phone: 929-444-9115
• Email: customerservice@compressinnovations.com
• Phone: 929-444-9115
• Email: customerservice@compressinnovations.com
• Phone: 929-444-9115
• Email: customerservice@compressinnovations.com
• Phone: 929-444-9115
• Email: customerservice@compressinnovations.com
• Phone: 929-444-9115
• Email: customerservice@compressinnovations.com
• Phone: 929-444-9115
• Email: customerservice@compressinnovations.com
• Phone: 929-444-9115
• Email: customerservice@compressinnovations.com
• Phone: 929-444-9115
• Email: customerservice@compressinnovations.com
• Phone: 929-444-9115
• Email: customerservice@compressinnovations.com
• Phone: 929-444-9115
• Email: customerservice@compressinnovations.com
• Phone: 929-444-9115
• Email: customerservice@compressinnovations.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860280002602 [Unit of Use]
GS1	10860280002609 [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: 2025-07-30
• Device Publish Date: 2025-07-22