K-2SM SmartMatt K-2SM-UMS

GUDID 00817012029390

Auto Immerssion, Alternating Pressure with On-Demand Low Air Loss Universal Mattress, Standard System

KAP MEDICAL

Low-air-loss bed Low-air-loss bed Low-air-loss bed Low-air-loss bed Low-air-loss bed Low-air-loss bed Low-air-loss bed Low-air-loss bed Low-air-loss bed Low-air-loss bed Low-air-loss bed Low-air-loss bed Low-air-loss bed Low-air-loss bed Low-air-loss bed

• Primary Device ID: 00817012029390
• NIH Device Record Key: d5e584a2-a66e-4b2f-94d8-1da03439ad5f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: K-2SM SmartMatt
• Version Model Number: K-2SM-UMS
• Catalog Number: K-2SM-UMS
• Company DUNS: 135241342
• Company Name: KAP MEDICAL
• 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: 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

Customer Support Contacts

• Phone: 951-340-4360
• Email: sales@kapmedical.com
• Phone: 951-340-4360
• Email: sales@kapmedical.com
• Phone: 951-340-4360
• Email: sales@kapmedical.com
• Phone: 951-340-4360
• Email: sales@kapmedical.com
• Phone: 951-340-4360
• Email: sales@kapmedical.com
• Phone: 951-340-4360
• Email: sales@kapmedical.com
• Phone: 951-340-4360
• Email: sales@kapmedical.com
• Phone: 951-340-4360
• Email: sales@kapmedical.com
• Phone: 951-340-4360
• Email: sales@kapmedical.com
• Phone: 951-340-4360
• Email: sales@kapmedical.com
• Phone: 951-340-4360
• Email: sales@kapmedical.com
• Phone: 951-340-4360
• Email: sales@kapmedical.com
• Phone: 951-340-4360
• Email: sales@kapmedical.com
• Phone: 951-340-4360
• Email: sales@kapmedical.com
• Phone: 951-340-4360
• Email: sales@kapmedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817012029390 [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: 2020-08-21
• Device Publish Date: 2020-08-13

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