SURELOCK, CURBELL, RED, 14 PK 27682

GUDID 00840828185912

SURELOCK, CURBELL, RED LEVER, 14 PACK

CURBELL MEDICAL PRODUCTS, INC.

Electrocardiographic electrode, reusable

• Primary Device ID: 00840828185912
• NIH Device Record Key: 0da67e36-74b9-4377-9064-9072974d0fa6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SURELOCK, CURBELL, RED, 14 PK
• Version Model Number: CL-10400-03-14
• Catalog Number: 27682
• Company DUNS: 796452311
• Company Name: CURBELL MEDICAL PRODUCTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com
• Phone: 1-800-235-7500
• Email: mwinter@curbell.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840828185912 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K080605

FDA Product Code

• DSA: Cable, Transducer And Electrode, Patient, (Including Connector)

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: 2022-04-27
• Device Publish Date: 2022-04-19

Devices Manufactured by CURBELL MEDICAL PRODUCTS, INC.

• 00840828195805 - GEN4 INTERACTIVE: 2025-12-24
• 00840828195812 - RESPONDER 5, INTERACTIVE: 2025-12-24
• 00840828195485 - RESPONDER 5, INTERACTIVE: 2025-12-17
• 00840828195492 - RESPONDER 5, INTERACTIVE: 2025-12-17
• 00840828195508 - GEN4 INTERACTIVE: 2025-12-17
• 00840828195515 - GEN4 INTERACTIVE: 2025-12-17
• 00840828195522 - GEN4 INTERACTIVE: 2025-12-17
• 00840828195539 - GEN4 INTERACTIVE: 2025-12-17