SecuriT 7502234

GUDID 10610075069900

2-Pc Ostomy System

HOLLISTER INCORPORATED

Multiple-piece urostomy bag, open-ended Multiple-piece urostomy bag, open-ended Multiple-piece urostomy bag, open-ended Multiple-piece urostomy bag, open-ended Multiple-piece urostomy bag, open-ended Multiple-piece urostomy bag, open-ended Multiple-piece urostomy bag, open-ended Multiple-piece urostomy bag, open-ended Multiple-piece urostomy bag, open-ended Multiple-piece urostomy bag, open-ended Multiple-piece urostomy bag, open-ended Multiple-piece urostomy bag, open-ended

• Primary Device ID: 10610075069900
• NIH Device Record Key: ef279a94-56d4-4e2f-a826-f972cf701260
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SecuriT
• Version Model Number: 7502234
• Catalog Number: 7502234
• Company DUNS: 005527098
• Company Name: HOLLISTER INCORPORATED
• Device Count: 10
• 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: false
• 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: false
• 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

Device Dimensions

• Lumen/Inner Diameter: 70 Millimeter
• Lumen/Inner Diameter: 70 Millimeter
• Lumen/Inner Diameter: 70 Millimeter
• Lumen/Inner Diameter: 70 Millimeter
• Lumen/Inner Diameter: 70 Millimeter
• Lumen/Inner Diameter: 70 Millimeter
• Lumen/Inner Diameter: 70 Millimeter
• Lumen/Inner Diameter: 70 Millimeter
• Lumen/Inner Diameter: 70 Millimeter
• Lumen/Inner Diameter: 70 Millimeter
• Lumen/Inner Diameter: 70 Millimeter
• Lumen/Inner Diameter: 70 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00610075069903 [Primary]
GS1	10610075069900 [Package]; Contains: 00610075069903; Package: CAS [12 Units]; In Commercial Distribution
GS1	20610075069907 [Unit of Use]

FDA Product Code

• EXG: BAG, URINE COLLECTING, URETEROSTOMY

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: 2022-12-09
• Device Publish Date: 2022-12-01

On-Brand Devices [SecuriT]

• 20610075068061: Ostomy Powder
• 20610075068054: Stoma Paste
• 20610075068047: Lubricating Gel Deodorant
• 20610075068023: Ostomy Deodorant
• 10610075084163: Stoma Paste
• 10610075069900: 2-Pc Ostomy System
• 10610075069504: Hydrocolloid Skin Barrier Strips