SteriCare Solutions

GUDID 00850421008822

NURSE ASSIST, INC.

Non-antimicrobial wound irrigation solution, saline, sterile Non-antimicrobial wound irrigation solution, saline, sterile Non-antimicrobial wound irrigation solution, saline, sterile Non-antimicrobial wound irrigation solution, saline, sterile Non-antimicrobial wound irrigation solution, saline, sterile Non-antimicrobial wound irrigation solution, saline, sterile Non-antimicrobial wound irrigation solution, saline, sterile Non-antimicrobial wound irrigation solution, saline, sterile Non-antimicrobial wound irrigation solution, saline, sterile Non-antimicrobial wound irrigation solution, saline, sterile Non-antimicrobial wound irrigation solution, saline, sterile Non-antimicrobial wound irrigation solution, saline Non-antimicrobial wound irrigation solution, saline Non-antimicrobial wound irrigation solution, saline Non-antimicrobial wound irrigation solution, saline Non-antimicrobial wound irrigation solution, saline Non-antimicrobial wound irrigation solution, saline Non-antimicrobial wound irrigation solution, saline Non-antimicrobial wound irrigation solution, saline Non-antimicrobial wound irrigation solution, saline Non-antimicrobial wound irrigation solution, saline Non-antimicrobial wound irrigation solution, saline

• Primary Device ID: 00850421008822
• NIH Device Record Key: fe597a4f-af28-457f-b2f7-7511c725ba51
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SteriCare Solutions
• Version Model Number: 6270
• Company DUNS: 869434464
• Company Name: NURSE ASSIST, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx
• Phone: 800-649-6800
• Email: xxx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850421008822 [Primary]
GS1	10850421008829 [Package]; Package: [24 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K083042

FDA Product Code

• FRO: Dressing, Wound, Drug

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-09-15
• Device Publish Date: 2021-09-07

On-Brand Devices [SteriCare Solutions]

• 00850421008785: 500 ML, USP STERILE WATER, BOTTLE
• 00850421008846: 6281
• 00850421008822: 6270
• 00850421008815: 6240
• 00850421008877: USP Normal Saline, 120 mL Cup
• 00850421008839: USP Normal Saline, 500 mL Bottle
• 00850421008754: USP Normal Saline, Would Flush, 3 oz
• 00850421008747: USP Normal Saline, Wound Flush, 7 oz
• B15064927750: USP Normal Saline, 100 mL Bottle
• 00850421008891: 500 ML, USP STERILE WATER, BOTTLE
• 00850421008198: USP Normal Saline, 500 mL Bottle