K-0SGS SkinGuard U-K-0SGS84

GUDID 00817012022698

SkinGuard Microclimate Control System, 84" Length

KAP MEDICAL

Low-air-loss bed

• Primary Device ID: 00817012022698
• NIH Device Record Key: 6cc37548-a087-4106-b271-c1a9b347b866
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: K-0SGS SkinGuard
• Version Model Number: U-K-0SGS84
• Catalog Number: U-K-0SGS84
• 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	00817012022698 [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: 2019-12-13
• Device Publish Date: 2019-12-05

On-Brand Devices [K-0SGS SkinGuard]

• 00817012022100: SkinGuard Microclimate Control System, 80" x 36"
• 00817012022698: SkinGuard Microclimate Control System, 84" Length
• 00817012022377: SkinGuard Microclimate Control System, 84"x 36"