ProcedureKitCRF CRF-U1505S-K

GUDID 00811746032992

CRF Procedure Kit

CAMBRIDGE INTERVENTIONAL LLC

Percutaneous radio-frequency ablation probe, tumour-ablation, monopolar

• Primary Device ID: 00811746032992
• NIH Device Record Key: 73ae022f-7edd-4587-bbaa-9c58f0575662
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ProcedureKitCRF
• Version Model Number: CRF-U1505S-K
• Catalog Number: CRF-U1505S-K
• 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00811746032992 [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: 2022-07-14
• Device Publish Date: 2022-07-06

On-Brand Devices [ProcedureKitCRF]

• 00811746032992: CRF Procedure Kit
• 00811746032985: CRF Procedure Kit
• 00811746032978: CRF Procedure Kit
• 00811746032961: CRF Procedure Kit
• 00811746032954: CRF Procedure Kit
• 00811746032947: CRF Procedure Kit
• 00811746032930: CRF Procedure Kit
• 00811746032923: CRF Procedure Kit
• 00811746032916: CRF Procedure Kit
• 00811746032909: CRF Procedure Kit
• 00811746032893: CRF Procedure Kit
• 00811746032886: CRF Procedure Kit
• 00811746032879: CRF Procedure Kit
• 00811746032862: CRF Procedure Kit
• 00811746032855: CRF Procedure Kit
• 00811746033142: CRF Procedure Kit
• 00811746033227: CRF Procedure Kit
• 00811746033210: CRF Procedure Kit
• 00811746033203: CRF Procedure Kit
• 00811746033197: CRF Procedure Kit
• 00811746033180: CRF Procedure Kit
• 00811746033173: CRF Procedure Kit
• 00811746033166: CRF Procedure Kit
• 00811746033159: CRF Procedure Kit
• 00811746033289: CRF Procedure Kit
• 00811746033272: CRF Procedure Kit
• 00811746033265: CRF Procedure Kit
• 00811746033258: CRF Procedure Kit
• 00811746033241: CRF Procedure Kit
• 00811746033234: CRF Procedure Kit