CHAIR PAD, 30-DAY, 10"X15", CORDED 17862

GUDID 00840828161541

CHAIR PAD, 30-DAY, 10"X15", CORDED

CURBELL MEDICAL PRODUCTS, INC.

Bed/chair occupancy sensor

• Primary Device ID: 00840828161541
• NIH Device Record Key: 311a6421-a30f-4dea-ae39-2ccb179e290b
• Commercial Distribution Discontinuation: 2019-12-23
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: CHAIR PAD, 30-DAY, 10"X15", CORDED
• Version Model Number: CSP-C30-NC10
• Catalog Number: 17862
• Company DUNS: 796452311
• Company Name: CURBELL MEDICAL PRODUCTS, INC.
• 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: true
• Serial Number: false
• 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: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com
• Phone: 18002357500
• Email: mwinter@curbell.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840828161541 [Primary]

FDA Product Code

• KMI: Monitor, Bed Patient

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: 2019-12-23
• Device Publish Date: 2019-04-19

Devices Manufactured by CURBELL MEDICAL PRODUCTS, INC.

• 00840828193733 - GEN4 DIRECT ACCESS: 2025-01-16
• 00840828193740 - GEN4 DIRECT ACCESS: 2025-01-16
• 00840828193757 - GEN4 DIRECT ACCESS: 2025-01-16
• 00840828193764 - GEN4 DIRECT ACCESS: 2025-01-16
• 00840828193771 - GEN4 INTERACTIVE: 2025-01-16
• 00840828193788 - GEN4 INTERACTIVE: 2025-01-16
• 00840828193795 - GEN4 INTERACTIVE: 2025-01-16
• 00840828193801 - GEN4 PLUS, DIRECT ACCESS: 2025-01-16