PHOSPHOR PLATE BARRIER ENVELOPES

GUDID D89260705533660

MAXILL, INC.

Digital imaging cassette

• Primary Device ID: D89260705533660
• NIH Device Record Key: 9e6e9d48-f394-49c9-9aa5-f2347ade8f20
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PHOSPHOR PLATE BARRIER ENVELOPES
• Version Model Number: 6070553366
• Company DUNS: 079343581
• Company Name: MAXILL, INC.
• Device Count: 10000
• 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: 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	D89260705533660 [Unit of Use]
HIBCC	D89260705533661 [Primary]
HIBCC	D89260705533662 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K163447

FDA Product Code

• PEM: Dental Barriers And Sleeves

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: 2022-08-01
• Device Publish Date: 2022-07-22

On-Brand Devices [PHOSPHOR PLATE BARRIER ENVELOPES]

• D89260705533670: 6070553367
• D89260705533660: 6070553366
• D89260705533650: 6070553365
• D89260705533620: 6070553362
• D89260705533610: 6070553361
• D89260705533600: 6070553360