Full-Length Face Shield

GUDID 00616784220925

Full-Length Face Shield

DYNAREX CORPORATION

Face splash shield, single-use

• Primary Device ID: 00616784220925
• NIH Device Record Key: a099f24d-0ced-44c0-87c8-833c5c13bcd4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Full-Length Face Shield
• Version Model Number: 2209
• Company DUNS: 008124539
• Company Name: DYNAREX CORPORATION
• Device Count: 40
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Safe
• 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	00616784220925 [Unit of Use]
GS1	00616784220932 [Primary]

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: 2021-04-30
• Device Publish Date: 2021-04-22

On-Brand Devices [Full-Length Face Shield]

• 00616784220925: Full-Length Face Shield
• 00810180843386: Full-Length Face Shield