OmniTrust 413-01

GUDID 50810572004567

OmniTrust Powder Free Synthetic Vinyl Examination Glove OEF Small

OMNI INTERNATIONAL CORP.

Vinyl examination/treatment glove, non-powdered

• Primary Device ID: 50810572004567
• NIH Device Record Key: dd8bd978-4aff-45df-929d-7d8917c64acf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OmniTrust
• Version Model Number: 413-01
• Catalog Number: 413-01
• Company DUNS: 079434709
• Company Name: OMNI INTERNATIONAL CORP.
• Device Count: 150
• 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: false

Customer Support Contacts

• Phone: 6034711499
• Email: Info@omnigloves.com
• Phone: 6034711499
• Email: Info@omnigloves.com
• Phone: 6034711499
• Email: Info@omnigloves.com
• Phone: 6034711499
• Email: Info@omnigloves.com
• Phone: 6034711499
• Email: Info@omnigloves.com
• Phone: 6034711499
• Email: Info@omnigloves.com
• Phone: 6034711499
• Email: Info@omnigloves.com
• Phone: 6034711499
• Email: Info@omnigloves.com
• Phone: 6034711499
• Email: Info@omnigloves.com
• Phone: 6034711499
• Email: Info@omnigloves.com
• Phone: 6034711499
• Email: Info@omnigloves.com
• Phone: 6034711499
• Email: Info@omnigloves.com
• Phone: 6034711499
• Email: Info@omnigloves.com
• Phone: 6034711499
• Email: Info@omnigloves.com
• Phone: 6034711499
• Email: Info@omnigloves.com
• Phone: 6034711499
• Email: Info@omnigloves.com
• Phone: 6034711499
• Email: Info@omnigloves.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810572004562 [Primary]
GS1	10810572004569 [Unit of Use]
GS1	50810572004567 [Package]; Contains: 00810572004562; Package: Shipper Carton [10 Units]; In Commercial Distribution

FDA Product Code

• LYZ: Vinyl 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: 2024-07-30
• Device Publish Date: 2024-07-22

On-Brand Devices [OmniTrust]

• 50810572004475: Nitrile Examination Gloves Powder Free XX-Large
• 50810572004468: Nitrile Examination Gloves Powder Free X-Large
• 50810572004451: Nitrile Examination Gloves Powder Free Large
• 50810572004444: Nitrile Examination Glove Powder Free Medium
• 50810572004437: Nitrile Examination Glove Powder Free Small
• 50810572004420: Nitrile Examination Glove Powder Free X-Small
• 50810572004536: Powder Free Nitrile Examination Gloves XX-Large
• 50810572004529: Powder Free Nitrile Examination Gloves X-Large
• 50810572004512: Powder Free Nitrile Examination Gloves Large
• 50810572004505: Powder Free Nitrile Examination Gloves Medium
• 50810572004499: Powder Free Nitrile Examination Gloves Small
• 50810572004482: Powder Free Nitrile Examination Gloves X-Small
• 50810572004598: OmniTrust Powder Free Synthetic Vinyl Examination Glove OEF X-Large
• 50810572004574: OmniTrust Powder Free Synthetic Vinyl Examination Glove OEF Medium
• 50810572004581: OmniTrust Powder Free Synthetic Vinyl Examination Glove OEF Large
• 50810572004567: OmniTrust Powder Free Synthetic Vinyl Examination Glove OEF Small
• 50810572004550: OmniTrust Powder Free Synthetic Vinyl Examination Glove OEF X-Small