IsoAir 2941-001-100

GUDID 07613327503999

STRYKER CORPORATION

Alternating-pressure bed mattress overlay system

• Primary Device ID: 07613327503999
• NIH Device Record Key: 2cce8c7e-a2eb-4664-9e2c-104675808d66
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IsoAir
• Version Model Number: 2941
• Catalog Number: 2941-001-100
• Company DUNS: 078470558
• Company Name: STRYKER CORPORATION
• 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: true
• 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

Operating and Storage Conditions

• Handling Environment Humidity: Between 30 Percent (%) Relative Humidity and 75 Percent (%) Relative Humidity

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327503999 [Primary]

FDA Product Code

• FNM: MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE

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: 2020-03-31
• Device Publish Date: 2020-03-23

On-Brand Devices [IsoAir]

• 07613327503999: 2941
• 07613327504002: 84 Inch System