CeraPlus 79402

GUDID 20610075092790

CeraPlus Barrier Extender

HOLLISTER INCORPORATED

Peristomal/periwound dressing Peristomal/periwound dressing Peristomal/periwound dressing Peristomal/periwound dressing Peristomal/periwound dressing Peristomal/periwound dressing Peristomal/periwound dressing Peristomal/periwound dressing Peristomal/periwound dressing Peristomal/periwound dressing Peristomal/periwound dressing Peristomal/periwound dressing Peristomal/periwound dressing Peristomal/periwound dressing Peristomal/periwound dressing Peristomal/periwound dressing

• Primary Device ID: 20610075092790
• NIH Device Record Key: 7f663ee9-a22d-45c2-90fa-2aaa0a72a7b5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CeraPlus
• Version Model Number: 79402
• Catalog Number: 79402
• Company DUNS: 005527098
• Company Name: HOLLISTER INCORPORATED
• Device Count: 30
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(800)323-4060
• Email: cs@hollister.com
• Phone: +1(800)323-4060
• Email: cs@hollister.com
• Phone: +1(800)323-4060
• Email: cs@hollister.com
• Phone: +1(800)323-4060
• Email: cs@hollister.com
• Phone: +1(800)323-4060
• Email: cs@hollister.com
• Phone: +1(800)323-4060
• Email: cs@hollister.com
• Phone: +1(800)323-4060
• Email: cs@hollister.com
• Phone: +1(800)323-4060
• Email: cs@hollister.com
• Phone: +1(800)323-4060
• Email: cs@hollister.com
• Phone: +1(800)323-4060
• Email: cs@hollister.com
• Phone: +1(800)323-4060
• Email: cs@hollister.com
• Phone: +1(800)323-4060
• Email: cs@hollister.com
• Phone: +1(800)323-4060
• Email: cs@hollister.com
• Phone: +1(800)323-4060
• Email: cs@hollister.com
• Phone: +1(800)323-4060
• Email: cs@hollister.com
• Phone: +1(800)323-4060
• Email: cs@hollister.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00610075092796 [Primary]
GS1	20610075092790 [Unit of Use]

FDA Product Code

• EXE: Protector, ostomy

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: 2023-05-22
• Device Publish Date: 2023-05-12

Devices Manufactured by HOLLISTER INCORPORATED

• 20610075104394 - InstantCath: 2024-07-17 Pre-lubricated Urethral Intermittent Catheter
• 20610075104400 - InstantCath: 2024-07-17 Pre-lubricated Urethral Intermittent Catheter
• 20610075104417 - InstantCath: 2024-07-17 Pre-lubricated Urethral Intermittent Catheter
• 25390166097587 - InstantCath: 2024-07-17 Pre-lubricated Urethral Intermittent Catheter
• 20610075104431 - InstantCath: 2024-07-17 Pre-lubricated Urethral Intermittent Catheter
• 20610075104448 - InstantCath: 2024-07-17 Pre-lubricated Urethral Intermittent Catheter
• 20610075104455 - InstantCath: 2024-07-17 Pre-lubricated Urethral Intermittent Catheter
• 20610075104479 - InstantCath: 2024-07-17 Pre-lubricated Urethral Intermittent Catheter