STERILIZATION TUBING

GUDID D89260705600451

MAXILL, INC.

Sterilization packaging, single-use

• Primary Device ID: D89260705600451
• NIH Device Record Key: b3f949e4-d0d3-48a9-b320-386c519d59a6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: STERILIZATION TUBING
• Version Model Number: 6070560045
• Company DUNS: 079343581
• Company Name: MAXILL, INC.
• Device Count: 1
• 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: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D89260705600450 [Primary]
HIBCC	D89260705600451 [Package]; Contains: D89260705600450; Package: Case [98 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K180661

FDA Product Code

• FRG: Wrap, Sterilization

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: 2022-09-27
• Device Publish Date: 2022-09-19

On-Brand Devices [STERILIZATION TUBING]

• D89260705600471: 6070560047
• D89260705600461: 6070560046
• D89260705600451: 6070560045