CaseGeneratorCRF CRF-SCG

GUDID 00811746030769

Radio-frequency ablation system

Primary Device ID	00811746030769
NIH Device Record Key	b7c22bda-940d-4081-9577-4cd69a7336db
Commercial Distribution Status	In Commercial Distribution
Brand Name	CaseGeneratorCRF
Version Model Number	CRF-SCG
Catalog Number	CRF-SCG
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

Device Issuing Agency	Device ID
GS1	00811746030769 [Primary]

GEI	Electrosurgical, Cutting & Coagulation & Accessories

Steralize Prior To Use	false
Device Is Sterile	false

10811746033293 - ElectrodeCRF	2024-10-28 CRF Radiofrequency Electrode
10811746033309 - ElectrodeCRF	2024-10-28 CRF Radiofrequency Electrode
10811746033316 - ElectrodeCRF	2024-10-28 CRF Radiofrequency Electrode
10811746033323 - ElectrodeCRF	2024-10-28 CRF Radiofrequency Electrode
10811746033330 - ElectrodeCRF	2024-10-28 CRF Radiofrequency Electrode
10811746033347 - ElectrodeCRF	2024-10-28 CRF Radiofrequency Electrode
10811746033354 - ElectrodeCRF	2024-10-28 CRF Radiofrequency Electrode
10811746033361 - ElectrodeCRF	2024-10-28 CRF Radiofrequency Electrode