Air+ 2863-000-000

GUDID 07613327499735

STRYKER CORPORATION

Flotation therapy bed, adult

• Primary Device ID: 07613327499735
• NIH Device Record Key: b9848824-c029-49ea-9fe2-a24841bc53ef
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Air+
• Version Model Number: 2863-000-000
• Catalog Number: 2863-000-000
• 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: true
• OTC Over-The-Counter: false

Operating and Storage Conditions

• Handling Environment Temperature: Between 50 Degrees Fahrenheit and 95 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327499735 [Primary]

FDA Product Code

• IOQ: BED, FLOTATION THERAPY, POWERED

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: 2019-10-24
• Device Publish Date: 2019-10-16

On-Brand Devices [Air+]

• 07613327499735: 2863-000-000
• 07613327482065: All-Inside Meniscal Repair System, Curved Up
• 07613327482072: All-Inside Meniscal Repair System, Curved Down