Endovapor® JSM120

GUDID 04250337105381

Electrosurgical system

Primary Device ID	04250337105381
NIH Device Record Key	591c2dc0-71db-43ef-948a-7cc434b71201
Commercial Distribution Status	In Commercial Distribution
Brand Name	Endovapor®
Version Model Number	JSM120
Catalog Number	JSM120
Company DUNS	344267187
Company Name	Joimax GmbH
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	true
Device Combination Product	false
Single Use	false
Lot Batch	false
Serial Number	true
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	04250337105381 [Primary]

GEI	Electrosurgical, cutting & coagulation & accessories

Steralize Prior To Use	false
Device Is Sterile	false

04250350109274	joimax® Neutral Electrode
04250337118848	joimax® Endovapor®2 System
04250337114604	joimax® Endovapor®2 System
04250337111832	joimax® Endovapor®2 System
04250337111825	joimax® Endovapor®2 System
04250337105626	joimax® Neutral Electrode Connecting Cable
04250337105381	joimax® Endovapor® Surgi-Max®
04250337103967	joimax® Endovapor®2 Device

Mark Image Registration \| Serial	Company Trademark Application Date
ENDOVAPOR 79103148 4223743 Live/Registered	Joimax GmbH 2011-08-08