CableAGP CRF-AGP

GUDID 00811746033029

Cable Adapter

CAMBRIDGE INTERVENTIONAL LLC

Electrosurgical cable adaptor
Primary Device ID00811746033029
NIH Device Record Key452765c2-53b2-4643-ae78-56840578a882
Commercial Distribution StatusIn Commercial Distribution
Brand NameCableAGP
Version Model NumberCRF-AGP
Catalog NumberCRF-AGP
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100811746033029 [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 Date2023-02-13
Device Publish Date2023-02-03

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10811746033361 - ElectrodeCRF2024-10-28 CRF Radiofrequency Electrode

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