K-ZZM ZMatt K-Z-ZM-AX-MS

GUDID 00817012030655

Rotation, Auto Immersion, Low Air Loss, Auto Expansion, Mattress System, 80"~85"~90"x 36"~42"~48"x 10".

KAP MEDICAL

Low-air-loss bed

• Primary Device ID: 00817012030655
• NIH Device Record Key: db7b1c50-c23b-44fb-8907-8e3d29888a0f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: K-ZZM ZMatt
• Version Model Number: K-Z-ZM-AX-MS
• Catalog Number: K-Z-ZM-AX-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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817012030655 [Primary]

FDA Product Code

• IKZ: Bed, Patient Rotation, 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: 2022-10-10
• Device Publish Date: 2022-09-30

On-Brand Devices [K-ZZM ZMatt]

• 00817012030655: Rotation, Auto Immersion, Low Air Loss, Auto Expansion, Mattress System, 80"~85"~90"x 36"~42"~48
• 00817012030648: Rotation, Low Air Loss, Auto Immersion, Auto Variable Length, Mattress System, 80"~85"~90"x 36"x