GUDID 00813250017793

G4 Test Lead for Reference Jack

BOSTON SCIENTIFIC NEUROMODULATION CORPORATION

Radio-frequency ablation system
Primary Device ID00813250017793
NIH Device Record Keyb55a4cb6-5d1d-40b6-96da-d26d61c0de3a
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberG4-TEST-REF
Company DUNS824951958
Company NameBOSTON SCIENTIFIC NEUROMODULATION CORPORATION
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100813250017793 [Primary]

FDA Product Code

GXDGENERATOR, LESION, RADIOFREQUENCY

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-10-08
Device Publish Date2017-08-21

Devices Manufactured by BOSTON SCIENTIFIC NEUROMODULATION CORPORATION

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