CableAPE CRF-APE

GUDID 00811746032718

Cable Adapter

CAMBRIDGE INTERVENTIONAL LLC

Radio-frequency ablation system
Primary Device ID00811746032718
NIH Device Record Key3605635f-42cc-423e-be84-40dc209fab17
Commercial Distribution StatusIn Commercial Distribution
Brand NameCableAPE
Version Model NumberCRF-APE
Catalog NumberCRF-APE
Company DUNS080897872
Company NameCAMBRIDGE INTERVENTIONAL LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com
Phone781-221-5300
Emailinfo@cambint.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100811746032718 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIElectrosurgical, Cutting & Coagulation & Accessories

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-04-08
Device Publish Date2022-03-31

Devices Manufactured by CAMBRIDGE INTERVENTIONAL LLC

10811746033293 - ElectrodeCRF2024-10-28 CRF Radiofrequency Electrode
10811746033309 - ElectrodeCRF2024-10-28 CRF Radiofrequency Electrode
10811746033316 - ElectrodeCRF2024-10-28 CRF Radiofrequency Electrode
10811746033323 - ElectrodeCRF2024-10-28 CRF Radiofrequency Electrode
10811746033330 - ElectrodeCRF2024-10-28 CRF Radiofrequency Electrode
10811746033347 - ElectrodeCRF2024-10-28 CRF Radiofrequency Electrode
10811746033354 - ElectrodeCRF2024-10-28 CRF Radiofrequency Electrode
10811746033361 - ElectrodeCRF2024-10-28 CRF Radiofrequency Electrode

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