GuideBlockCRF-C CRF-GBC

GUDID 10811746030681

Radio-frequency ablation system

Primary Device ID	10811746030681
NIH Device Record Key	a139d7b8-687d-4c5b-82c9-b88e6cc65314
Commercial Distribution Status	In Commercial Distribution
Brand Name	GuideBlockCRF-C
Version Model Number	CRF-GBC
Catalog Number	CRF-GBC
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	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

Device Issuing Agency	Device ID
GS1	00811746030684 [Primary]
GS1	10811746030681 [Package] Contains: 00811746030684 Package: [5 Units] In Commercial Distribution

GEI	Electrosurgical, Cutting & Coagulation & Accessories

Steralize Prior To Use	false
Device Is Sterile	true

00811746033395 - CableASE	2024-12-16 Cable Adapter
00811746033401 - CableA1E	2024-12-16 Cable Adapter
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