CHAIR PAD, WIRELESS,14-DAY, 7"X15" 19588

GUDID 00840828161602

CHAIR PAD, WIRELESS,14-DAY, 7"X15"

CURBELL MEDICAL PRODUCTS, INC.

Bed/chair occupancy sensor

• Primary Device ID: 00840828161602
• NIH Device Record Key: 27ac22ed-f100-44bb-8096-87ff6dd8d119
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CHAIR PAD, WIRELESS,14-DAY, 7"X15"
• Version Model Number: CSP-C14-NW7
• Catalog Number: 19588
• 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	00840828161602 [Primary]

FDA Product Code

• KMI: Monitor, Bed Patient

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: 2019-04-29
• Device Publish Date: 2019-04-19

Devices Manufactured by CURBELL MEDICAL PRODUCTS, INC.

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• 00840828194013 - RESPONDER 5, INTERACTIVE: 2025-02-24
• 00840828194020 - RESPONDER 5, STANDARD: 2025-02-24
• 00840828194037 - RESPONDER 5, STANDARD: 2025-02-24
• 00840828194044 - RESPONDER 5, STANDARD: 2025-02-24
• 00840828194051 - RESPONDER 5, INTERACTIVE: 2025-02-24
• 00840828194068 - RESPONDER 5, STANDARD: 2025-02-24