Canady Plasma GIT Probe

GUDID B413AW4225380

The Canady Hybrid Plasma Scalpel is an electrosurgical plasma probe that is 2.3mm in diameter and 3.4m long. The electrosurgical plasma probe is used

US MEDICAL INNOVATIONS, LLC

Argon-enhanced endoscopic electrosurgical electrode, single-use Argon-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use Inert gas-enhanced endoscopic electrosurgical electrode, single-use
Primary Device IDB413AW4225380
NIH Device Record Key96513943-a0b4-4987-9031-e7ae9a770964
Commercial Distribution StatusIn Commercial Distribution
Brand NameCanady Plasma GIT Probe
Version Model NumberAW-422538
Company DUNS961656951
Company NameUS MEDICAL INNOVATIONS, 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 Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB413AW4225380 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIElectrosurgical, Cutting & Coagulation & Accessories

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[B413AW4225380]

Ethylene Oxide


[B413AW4225380]

Ethylene Oxide


[B413AW4225380]

Ethylene Oxide


[B413AW4225380]

Ethylene Oxide


[B413AW4225380]

Ethylene Oxide


[B413AW4225380]

Ethylene Oxide


[B413AW4225380]

Ethylene Oxide


[B413AW4225380]

Ethylene Oxide


[B413AW4225380]

Ethylene Oxide


[B413AW4225380]

Ethylene Oxide


[B413AW4225380]

Ethylene Oxide


[B413AW4225380]

Ethylene Oxide


[B413AW4225380]

Ethylene Oxide


[B413AW4225380]

Ethylene Oxide


[B413AW4225380]

Ethylene Oxide


[B413AW4225380]

Ethylene Oxide


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number2
Public Version Date2018-07-06
Device Publish Date2018-03-05

Devices Manufactured by US MEDICAL INNOVATIONS, LLC

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B413AW4225380 - Canady Plasma GIT Probe2018-07-06 The Canady Hybrid Plasma Scalpel is an electrosurgical plasma probe that is 2.3mm in diameter and 3.4m long. The electrosurgical
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