K-0SGS SKINGUARD K-0SGS

GUDID 00817012022100

SkinGuard Microclimate Control System, 80" x 36"

KAP MEDICAL

Low-air-loss bed

• Primary Device ID: 00817012022100
• NIH Device Record Key: ce97b199-81cd-4f9b-94df-2fd20bdb3044
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: K-0SGS SKINGUARD
• Version Model Number: K-0SGS
• Catalog Number: K-0SGS
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817012022100 [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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-09-19

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"