CasePumpCRF CRF-SCP

GUDID 00811746030776

CRF Pump Storage Case

CAMBRIDGE INTERVENTIONAL LLC

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• Primary Device ID: 00811746030776
• NIH Device Record Key: 62663db2-1f6f-49c8-b8a7-63881d0e4e5d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CasePumpCRF
• Version Model Number: CRF-SCP
• Catalog Number: CRF-SCP
• 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
• Phone: 781-221-5300
• Email: info@cambint.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00811746030776 [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

• 00811746033159 - ProcedureKitCRF: 2023-08-08 CRF Procedure Kit
• 00811746033166 - ProcedureKitCRF: 2023-08-08 CRF Procedure Kit
• 00811746033173 - ProcedureKitCRF: 2023-08-08 CRF Procedure Kit
• 00811746033180 - ProcedureKitCRF: 2023-08-08 CRF Procedure Kit
• 00811746033197 - ProcedureKitCRF: 2023-08-08 CRF Procedure Kit
• 00811746033203 - ProcedureKitCRF: 2023-08-08 CRF Procedure Kit
• 00811746033210 - ProcedureKitCRF: 2023-08-08 CRF Procedure Kit
• 00811746033227 - ProcedureKitCRF: 2023-08-08 CRF Procedure Kit