AUTOCLAVE TAPE

GUDID D89260705600581

MAXILL, INC.

Chemical/physical sterilization process indicator

• Primary Device ID: D89260705600581
• NIH Device Record Key: d9f5a85a-ad4a-4b5c-9027-88d9fb384939
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AUTOCLAVE TAPE
• Version Model Number: 6070560058
• 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	D89260705600580 [Primary]
HIBCC	D89260705600581 [Package]; Contains: D89260705600580; Package: CASE [72 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K171823

FDA Product Code

• JOJ: Indicator, Physical/Chemical Sterilization Process

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 [AUTOCLAVE TAPE]

• D89260705600591: 6070560059
• D89260705600581: 6070560058
• D89260705600571: 6070560057