4022

GUDID 10884521527430

Clear Adhesive Bandage

Cardinal Health, Inc.

Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage Adhesive bandage

• Primary Device ID: 10884521527430
• NIH Device Record Key: 37e4df9a-0447-4edd-b64e-fde8f57e9c2a
• Commercial Distribution Discontinuation: 2025-12-31
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 4022
• Catalog Number: 4022
• Company DUNS: 080935429
• Company Name: Cardinal Health, Inc.
• Device Count: 10000
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry

Device Identifiers

Device Issuing Agency	Device ID
GS1	10884521527430 [Primary]
GS1	20884521527437 [Unit of Use]

FDA Product Code

• KGX: Tape and bandage, adhesive

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: 2023-12-08
• Device Publish Date: 2018-06-27

Devices Manufactured by Cardinal Health, Inc.

• 30884521013418 - Monoject: 2024-04-05 1 mL Tuberculin Syringe,Luer-Lock Tip
• 20884521010007 - Monoject: 2024-03-21 12 mL Syringe,Luer-Lock Tip
• 20884521740690 - Salem Sump: 2024-03-19 SILICONE SALEM SUMP ENFIT 10FR 36IN
• 20884521740706 - Salem Sump: 2024-03-19 SILICONE SALEM SUMP WITH ENFIT 12FR 48IN
• 20884521740713 - Salem Sump: 2024-03-19 SILICONE SALEM SUMP WITH ENFIT 14FR 48IN
• 20884521740720 - Salem Sump: 2024-03-19 SILICONE SALEM SUMP WITH ENFIT 16FR 48IN
• 20884521740737 - Salem Sump: 2024-03-19 SILICONE SALEM SUMP WITH ENFIT 18FR 48IN
• 20884521065229 - Telfa: 2024-03-12 Non-adherent Pads Prepack