K-4 D3X K-4-AW2.0-BB-X-MS

GUDID 00817012031133

Advanced Wave, Injection Molded Housing, Battery Backup, Alternating Pressure, Wave/Pulsating, True Low Air Loss, Width Expansion and Length Extension, Mattress System, 80"~85~90" x 36"~42"~48" x 10".

KAP MEDICAL

Low-air-loss bed

• Primary Device ID: 00817012031133
• NIH Device Record Key: 817d8d2d-eb36-4ec0-a22b-5d23f338cd8c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: K-4 D3X
• Version Model Number: K-4-AW2.0-BB-X-MS
• Catalog Number: K-4-AW2.0-BB-X-MS
• 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
• Phone: 951-340-4360
• Email: sales@kapmedical.com
• Phone: 951-340-4360
• Email: sales@kapmedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817012031133 [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: 2023-03-27
• Device Publish Date: 2023-03-17

On-Brand Devices [K-4 D3X ]

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• 00817012030235: Alternating Pressure, Low Air Loss, Mattress System, 84"x43"x10".
• 00817012030501: Alternating Pressure, Pulsating, True Low Air Loss, AutoSet, Auto Variable Length, Battery Backu
• 00817012030594: Alternating Pressure, Pulsating, Low Air Loss, Auto Variable Length, Mattress System, 80"~85"~90
• 00817012031133: Advanced Wave, Injection Molded Housing, Battery Backup, Alternating Pressure, Wave/Pulsating, T
• 00817012031126: Advanced Wave, Injection Molded Housing, Battery Backup, Alternating Pressure, Wave/Pulsating, T
• 00817012031119: Advanced Wave, Injection Molded Housing, Battery Backup, Alternating Pressure, Wave/Pulsating, T
• 00817012031102: Advanced Wave, Injection Molded Housing, Battery Backup, Alternating Pressure, Wave/Pulsating, T
• 00817012031195: Alternating Pressure, True Low Air loss, AutoSet, Pulsating, Auto Width and Length Expansion, Ma
• 00817012031539: Alternating Pressure, Battery Backup, True Low Air loss, AutoSet, Pulsating, Auto Width and Leng
• 00817012031560: Alternating Pressure, Pulsating, True Low Air Loss, Battery Backup, Mattress System, 80"x36"x8".
• 00817012031553: Alternating Pressure, Pulsating, True Low Air Loss, Battery Backup, Mattress System, 80"x36"x10"
• 00817012031645: Alternating Pressure, True Low Air Loss, Battery Backup, Mattress System, 80"x36"x8".