Dermatec Twilight GL+602STNITRILE

GUDID 10813417020649

Dermatec Twilight Blue Stretch Nitrile PF exam glove large 100/box, 10 box/case

Relda, Llc.

Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial

• Primary Device ID: 10813417020649
• NIH Device Record Key: 860ad2a0-169e-43e9-8448-1cc2c01f2a45
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dermatec Twilight
• Version Model Number: GL+602STNITRILE
• Catalog Number: GL+602STNITRILE
• Company DUNS: 101926900
• Company Name: Relda, Llc.
• Device Count: 100
• 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: false
• 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: (800) 992-8987
• Email: rmoney@dermatec.net
• Phone: (800) 992-8987
• Email: rmoney@dermatec.net
• Phone: (800) 992-8987
• Email: rmoney@dermatec.net
• Phone: (800) 992-8987
• Email: rmoney@dermatec.net
• Phone: (800) 992-8987
• Email: rmoney@dermatec.net
• Phone: (800) 992-8987
• Email: rmoney@dermatec.net
• Phone: (800) 992-8987
• Email: rmoney@dermatec.net
• Phone: (800) 992-8987
• Email: rmoney@dermatec.net
• Phone: (800) 992-8987
• Email: rmoney@dermatec.net
• Phone: (800) 992-8987
• Email: rmoney@dermatec.net
• Phone: (800) 992-8987
• Email: rmoney@dermatec.net
• Phone: (800) 992-8987
• Email: rmoney@dermatec.net
• Phone: (800) 992-8987
• Email: rmoney@dermatec.net
• Phone: (800) 992-8987
• Email: rmoney@dermatec.net
• Phone: (800) 992-8987
• Email: rmoney@dermatec.net

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813417020642 [Primary]
GS1	10813417020649 [Package]; Contains: 00813417020642; Package: box [10 Units]; In Commercial Distribution
GS1	70813417020641 [Unit of Use]

FDA Product Code

• LZA: Polymer Patient Examination Glove

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: 2022-09-13
• Device Publish Date: 2022-09-05

On-Brand Devices [Dermatec Twilight]

• 10813417020656: Dermatec Twilight Blue Stretch Nitrile PF exam glove xlarge 100/box, 10 box/case
• 10813417020649: Dermatec Twilight Blue Stretch Nitrile PF exam glove large 100/box, 10 box/case
• 10813417020632: Dermatec Twilight Blue Stretch Nitrile PF exam glove medium 100/box, 10 box/case
• 10813417020625: Dermatec Twilight Blue Stretch Nitrile PF exam glove small 100/box, 10 box/case
• 10813417020618: Dermatec Twilight Blue Stretch Nitrile PF exam glove xsmall 100/box, 10 box/case