Electrode Extender

GUDID GYNX1200001

GYNEX CORPORATION

Electrocautery system electrode
Primary Device IDGYNX1200001
NIH Device Record Key4b0023e6-ac0b-4d7e-aeb8-af44aff02b20
Commercial Distribution StatusIn Commercial Distribution
Brand NameElectrode Extender
Version Model Number12-0000
Company DUNS012997685
Company NameGYNEX CORPORATION
Device Count5
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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCGYNX1200000 [Unit of Use]
HIBCCGYNX1200001 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HGIElectrocautery, Gynecologic (And Accessories)

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-10-04

Devices Manufactured by GYNEX CORPORATION

GYNX16000 - Gynex2024-01-03
GYNX291000 - Gynex2024-01-03
GYNX292000 - Gynex2024-01-03
GYNX293500 - Gynex2024-01-03
GYNX295500 - Gynex2024-01-03
GYNX297000 - Gynex2024-01-03
GYNX298000 - Gynex2024-01-03
GYNX298500 - Gynex2024-01-03

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.