Reprocessed 3.5mm VAPR Side Effect Electrode

GUDID B3902253011

3.5mm VAPR Side Effect Electrode

SURETEK MEDICAL

Endoscopic electrosurgical handpiece/electrode, bipolar, reprocessed
Primary Device IDB3902253011
NIH Device Record Key8e2fbf87-8977-43da-a2b4-55a470239cce
Commercial Distribution StatusIn Commercial Distribution
Brand NameReprocessed 3.5mm VAPR Side Effect Electrode
Version Model Number225301
Company DUNS785616934
Company NameSURETEK MEDICAL
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

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB3902253011 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NUJElectrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-08-13
Device Publish Date2020-08-05

On-Brand Devices [Reprocessed 3.5mm VAPR Side Effect Electrode]

B3902273011227301
B39022530113.5mm VAPR Side Effect Electrode

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