maxill Frames Eyewear

GUDID D89260705532601

MAXILL, INC.

Eye splash shield, reusable

• Primary Device ID: D89260705532601
• NIH Device Record Key: 825d0627-f339-4a9f-8d2f-fee7ef1603c7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: maxill Frames Eyewear
• Version Model Number: 6070553260
• Company DUNS: 079343581
• Company Name: MAXILL, INC.
• Device Count: 1
• 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: false
• 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
HIBCC	D89260705532600 [Primary]
HIBCC	D89260705532601 [Package]; Contains: D89260705532600; Package: Box [6 Units]; In Commercial Distribution
HIBCC	D89260705532602 [Package]; Package: Case [324 Units]; In Commercial Distribution

FDA Product Code

• KPY: Shield, Protective, Personnel

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: 2022-11-22
• Device Publish Date: 2022-11-14

On-Brand Devices [maxill Frames Eyewear]

• D89260705532631: 6070553263
• D89260705532601: 6070553260