NitriDerm® EP Orange®

GUDID 10813172020946

Gloves, Exam, Nitrile, Chemo, Non-Sterile, Powder-Free, Textured, Ext Cuff, Orange, 6.5 mil, XXXL

INNOVATIVE HEALTHCARE CORPORATION

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

• Primary Device ID: 10813172020946
• NIH Device Record Key: 69e17556-05e4-4564-a63b-5ae376930110
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NitriDerm® EP Orange®
• Version Model Number: 189450
• Company DUNS: 802020693
• Company Name: INNOVATIVE HEALTHCARE CORPORATION
• Device Count: 80
• 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813172020949 [Unit of Use]
GS1	10813172020946 [Package]; Contains: 20813172020943; Package: 80/bx, 10 bx/cs [10 Units]; In Commercial Distribution
GS1	20813172020943 [Primary]

FDA Product Code

• LZA: Polymer Patient Examination Glove

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-05-21
• Device Publish Date: 2022-12-08

On-Brand Devices [NitriDerm® EP Orange®]

• 10813172020946: Gloves, Exam, Nitrile, Chemo, Non-Sterile, Powder-Free, Textured, Ext Cuff, Orange, 6.5 mil, XXX
• 10813172020939: Gloves, Exam, Nitrile, Chemo, Non-Sterile, Powder-Free, Textured, Ext Cuff, Orange, 6.5 mil, XXL
• 10813172020892: Gloves, Exam, Nitrile, Chemo, Non-Sterile, Powder-Free, Textured, Ext Cuff, Orange, 6.5 mil, S