SURE LOCK,A34,10 PK,ORANGE LEVER,CARDIOLINE 26873

GUDID 00840828183390

SURE LOCK,A34,10 PK,ORANGE LEVER,CARDIOLINE

CURBELL MEDICAL PRODUCTS, INC.

Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable Electrocardiographic electrode, reusable

• Primary Device ID: 00840828183390
• NIH Device Record Key: c411571e-8660-4cbd-ac96-403c88c00619
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SURE LOCK,A34,10 PK,ORANGE LEVER,CARDIOLINE
• Version Model Number: CL-10403-04-10
• Catalog Number: 26873
• 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
• 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	00840828183390 [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: 2021-05-05
• Device Publish Date: 2021-04-27

Devices Manufactured by CURBELL MEDICAL PRODUCTS, INC.

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• 00840828187756 - RLW,3PK,SNAP,SAFETY DIN,40",AHA: 2024-06-06 RLW,3PK,SNAP,SAFETY DIN,40",AHA
• 00840828187763 - RLW,5PK,SNAP,SAFETY DIN,18",AHA: 2024-06-06 RLW,5PK,SNAP,SAFETY DIN,18",AHA
• 00840828187770 - RLW,5PK,SNAP,SAFETY DIN,24",AHA: 2024-06-06 RLW,5PK,SNAP,SAFETY DIN,24",AHA
• 00840828187787 - RLW,5PK,SNAP,SAFETY DIN,40",AHA: 2024-06-06 RLW,5PK,SNAP,SAFETY DIN,40",AHA
• 00840828187947 - RLW,3PK,PINCH,SAFETY DIN,24",AHA: 2024-06-06 RLW,3PK,PINCH,SAFETY DIN,24",AHA
• 00840828187954 - RLW,3PK,PINCH,SAFETY DIN,40",AHA: 2024-06-06 RLW,3PK,PINCH,SAFETY DIN,40",AHA
• 00840828187961 - RLW,5PK,PINCH,SAFETY DIN,24",AHA: 2024-06-06 RLW,5PK,PINCH,SAFETY DIN,24",AHA