GroundPadCRF CRF-GP

GUDID 10811746030261

CRF Ground Pad

CAMBRIDGE INTERVENTIONAL LLC

Radio-frequency ablation system Electrosurgical return electrode, single-use Electrosurgical return electrode, single-use Electrosurgical return electrode, single-use Electrosurgical return electrode, single-use Electrosurgical return electrode, single-use Electrosurgical return electrode, single-use Electrosurgical return electrode, single-use Electrosurgical return electrode, single-use Electrosurgical return electrode, single-use Electrosurgical return electrode, single-use Electrosurgical return electrode, single-use Electrosurgical return electrode, single-use Electrosurgical return electrode, single-use Electrosurgical return electrode, single-use Electrosurgical return electrode, single-use Electrosurgical return electrode, single-use Electrosurgical return electrode, single-use
Primary Device ID10811746030261
NIH Device Record Key16b4152d-2b29-4653-970f-3d6e1f793a56
Commercial Distribution StatusIn Commercial Distribution
Brand NameGroundPadCRF
Version Model NumberCRF-GP
Catalog NumberCRF-GP
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100811746030264 [Primary]
GS110811746030261 [Package]
Contains: 00811746030264
Package: [25 Units]
In Commercial Distribution

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 Date2020-05-08
Device Publish Date2020-04-30

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