DLX Disposable Face Shield

GUDID 30850015055226

ULINE, INC.

Face splash shield, single-use

• Primary Device ID: 30850015055226
• NIH Device Record Key: b25e11af-f698-4ab6-b5bf-221361d97391
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DLX Disposable Face Shield
• Version Model Number: S-24607
• Company DUNS: 039612668
• Company Name: ULINE, 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: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850015055287 [Unit of Use]
GS1	10850015055284 [Primary]
GS1	30850015055226 [Package]; Contains: 10850015055284; Package: [4 Units]; In Commercial Distribution

FDA Product Code

• LYU: Accessory, Surgical Apparel

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: 2022-02-01
• Device Publish Date: 2022-01-24

Devices Manufactured by ULINE, INC.

• 30850015055509 - ULINE REUSABLE EARPLUGS - UNCORDED: 2024-08-02
• 30850015055516 - ULINE REUSABLE EARPLUGS - CORDED: 2024-08-02
• 30850015055523 - ULINE BULLET EARPLUGS - UNCORDED: 2024-07-31
• 30850015055530 - ULINE BULLET EARPLUGS - CORDED: 2024-07-31
• 30850015055547 - ULINE BELL EARPLUGS - UNCORDED: 2024-07-31
• 30850015055554 - ULINE BELL EARPLUGS - CORDED: 2024-07-31
• 30850015055493 - ULINE BULLET EARPLUGS REFILL: 2024-05-21
• 00850015055713 - ULINE EARPLUGS IN A BUCKET: 2024-05-21