PACKARD HEALTHCARE SELF SEALING STERILIZATION POUCHES

GUDID D89260705601802

MAXILL, INC.

Sterilization packaging, single-use

• Primary Device ID: D89260705601802
• NIH Device Record Key: 540ee46a-c288-44ab-9dfb-7ea025211adb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PACKARD HEALTHCARE SELF SEALING STERILIZATION POUCHES
• Version Model Number: 6070560180
• Company DUNS: 079343581
• Company Name: MAXILL, INC.
• Device Count: 200
• 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	D89260705601800 [Unit of Use]
HIBCC	D89260705601801 [Primary]
HIBCC	D89260705601802 [Package]; Contains: D89260705601801; Package: Case [2000 Units]; In Commercial Distribution

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: 2024-01-22
• Device Publish Date: 2024-01-12

On-Brand Devices [PACKARD HEALTHCARE SELF SEALING STERILIZATION POUCHES]

• D89260705601872: 6070560187
• D89260705601862: 6070560186
• D89260705601852: 6070560185
• D89260705601842: 6070560184
• D89260705601832: 6070560183
• D89260705601822: 6070560182
• D89260705601812: 6070560181
• D89260705601802: 6070560180