ProcedureKitCRF CRF-U1530-K

GUDID 00811746033234

CRF Procedure Kit

CAMBRIDGE INTERVENTIONAL LLC

Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar
Primary Device ID00811746033234
NIH Device Record Keyffa6c6bd-8c66-4331-b2bb-e72ebb20139b
Commercial Distribution StatusIn Commercial Distribution
Brand NameProcedureKitCRF
Version Model NumberCRF-U1530-K
Catalog NumberCRF-U1530-K
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 Kittrue
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100811746033234 [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 Date2024-09-09
Device Publish Date2024-08-31

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