PowerCordEU CRF-PEU

GUDID 00811746030721

CRF Power Cord

CAMBRIDGE INTERVENTIONAL LLC

Radio-frequency ablation system

• Primary Device ID: 00811746030721
• NIH Device Record Key: a70dde28-eb2e-41e6-8f6a-951914c4db05
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PowerCordEU
• Version Model Number: CRF-PEU
• Catalog Number: CRF-PEU
• Company DUNS: 080897872
• Company Name: CAMBRIDGE INTERVENTIONAL LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 781-221-5300
• Email: info@cambint.com
• Phone: 781-221-5300
• Email: info@cambint.com
• Phone: 781-221-5300
• Email: info@cambint.com
• Phone: 781-221-5300
• Email: info@cambint.com
• Phone: 781-221-5300
• Email: info@cambint.com
• Phone: 781-221-5300
• Email: info@cambint.com
• Phone: 781-221-5300
• Email: info@cambint.com
• Phone: 781-221-5300
• Email: info@cambint.com
• Phone: 781-221-5300
• Email: info@cambint.com
• Phone: 781-221-5300
• Email: info@cambint.com
• Phone: 781-221-5300
• Email: info@cambint.com
• Phone: 781-221-5300
• Email: info@cambint.com
• Phone: 781-221-5300
• Email: info@cambint.com
• Phone: 781-221-5300
• Email: info@cambint.com
• Phone: 781-221-5300
• Email: info@cambint.com
• Phone: 781-221-5300
• Email: info@cambint.com
• Phone: 781-221-5300
• Email: info@cambint.com
• Phone: 781-221-5300
• Email: info@cambint.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00811746030721 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K192715

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

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: 2020-05-08
• Device Publish Date: 2020-04-30

Devices Manufactured by CAMBRIDGE INTERVENTIONAL LLC

• 00811746033418 - ProcedureKitCRF: 2026-01-21 CRF Procedure Kit
• 00811746033425 - ProcedureKitCRF: 2026-01-21 CRF Procedure Kit
• 00811746033432 - ProcedureKitCRF: 2026-01-21 CRF Procedure Kit
• 00811746033449 - ProcedureKitCRF: 2026-01-21 CRF Procedure Kit
• 00811746033456 - ProcedureKitCRF: 2026-01-21 CRF Procedure Kit
• 00811746033463 - ProcedureKitCRF: 2026-01-21 CRF Procedure Kit
• 00811746033470 - ProcedureKitCRF: 2026-01-21 CRF Procedure Kit
• 00811746033487 - ProcedureKitCRF: 2026-01-21 CRF Procedure Kit