SureCare® DUP82911

GUDID 00809958084014

3 in X 2 in non-woven eye pad

Derma Sciences Canada Inc

Eye pad

• Primary Device ID: 00809958084014
• NIH Device Record Key: f76c0e5e-ec6a-4579-ad65-150399bb7df5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SureCare®
• Version Model Number: 82911
• Catalog Number: DUP82911
• Company DUNS: 200564891
• Company Name: Derma Sciences Canada Inc
• Device Count: 25
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com

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 Identifiers

Device Issuing Agency	Device ID
GS1	00809958084007 [Unit of Use]
GS1	00809958084014 [Primary]

FDA Product Code

• HMP: PAD, EYE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-03-21
• Device Publish Date: 2018-10-23

Devices Manufactured by Derma Sciences Canada Inc

• 00809958187968 - ALGICELL® Ag: 2025-01-16 ALGICELL AG CALCIUM ALGINATE SILVER 2"X 2"
• 00809958187982 - ALGICELL® Ag: 2025-01-16 SILVER ALGINATE 4.25"X 4.25" DRESSING
• 00809958188002 - ALGICELL® Ag: 2025-01-16 ALGICELL AG CALCIUM ALGINATE SILVER 4"X 5"
• 00809958001905 - ALGICELL® Ag: 2025-01-16 ALGICELL AG CALCIUM ALGINATE SILVER 4"X 8"
• 00809958188040 - ALGICELL® Ag: 2025-01-16 ALGICELL AG CALCIUM ALGINATE SILVER 8"X 12"
• 00809958001844 - ALGICELL® Ag: 2025-01-15 ALGICELL AG CALCIUM ALGINATE SILVER 3/4"X 12" ROPE
• 30381780491709 - PETROLATUM GAUZE®: 2024-06-25 Petrolatum Gauze Non-Adhering Dressing
• 30381780491716 - PETROLATUM GAUZE®: 2024-06-25 Petrolatum Gauze Non-Adhering Dressing