Action

GUDID 00641932360130

Action 36000 Black Nitrile Examination Powder Free Textured Gloves, Large

Shamrock Marketing Co., Inc.

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

• Primary Device ID: 00641932360130
• NIH Device Record Key: d386a179-f704-45e4-8d8d-ce64eec3054a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Action
• Version Model Number: 36013
• Company DUNS: 010206618
• Company Name: Shamrock Marketing Co., 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00641932360130 [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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-09-25
• Device Publish Date: 2023-09-15

On-Brand Devices [Action]

• 00641932360147: Action 36000 Black Nitrile Examination Powder Free Textured Gloves, Xlarge
• 00641932360130: Action 36000 Black Nitrile Examination Powder Free Textured Gloves, Large
• 00641932360123: Action 36000 Black Nitrile Examination Powder Free Textured Gloves, Medium
• 00641932360116: Action 36000 Black Nitrile Examination Powder Free Textured Gloves, Small
• 00641932177042: Action 17700 Latex Examination Powder Free Textured Gloves, XLarge
• 00641932177035: Action 17700 Latex Examination Powder Free Textured Gloves, Large
• 00641932177028: Action 17700 Latex Examination Powder Free Textured Gloves, Medium
• 00641932177011: Action 17700 Latex Examination Powder Free Textured Gloves, Small