CARDINAL HEALTH ST-HM39SPU-HLF-B

GUDID 50885380168510

Hovertech Hovermatt Lateral Transfer Mattress

Cardinal Health, Inc.

Patient transfer system, powered

• Primary Device ID: 50885380168510
• NIH Device Record Key: 80b8cf67-a2f7-46c0-8a75-944ef1d1c3d2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CARDINAL HEALTH
• Version Model Number: ST-HM39SPU-HLF-B
• Catalog Number: ST-HM39SPU-HLF-B
• Company DUNS: 080935429
• Company Name: Cardinal Health, Inc.
• 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: true
• Lot Batch: false
• Serial Number: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10885380168512 [Primary]
GS1	50885380168510 [Package]; Contains: 10885380168512; Package: CASE [10 Units]; In Commercial Distribution

FDA Product Code

• FRZ: DEVICE, PATIENT TRANSFER, 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: 2019-10-11
• Device Publish Date: 2019-10-03

On-Brand Devices [CARDINAL HEALTH]

• 50885380041233: Cardinal Health Adult Briefs Maximum Absorbency
• 50885380159235: UNDERPAD EXTRA ABSORBENCY 30 X 36IN
• 50885380159228: UNDERPAD EXTRA ABSORBENCY 24 X 36IN
• 50885380168527: Hovertech Hovermatt Lateral Transfer Mattress
• 50885380168510: Hovertech Hovermatt Lateral Transfer Mattress
• 50885380168503: Hovertech Hovermatt Lateral Transfer Mattress
• 50885380168497: Hovertech Hovermatt Lateral Transfer Mattress
• 50885380168480: Hovertech Hovermatt Lateral Transfer Mattress