VS3 Iridium 153-0073RFB

GUDID 10813040013261

VS3 Iridium Endoscope-IR 10mm, Long, 0°, Standard FOV - Refurbished

VISIONSENSE LTD.

Endoscope video camera
Primary Device ID10813040013261
NIH Device Record Key96f26f92-c59a-457c-85ae-4250cf623856
Commercial Distribution StatusIn Commercial Distribution
Brand NameVS3 Iridium
Version Model NumberVS3-IR
Catalog Number153-0073RFB
Company DUNS532199478
Company NameVISIONSENSE LTD.
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 Batchfalse
Serial Numbertrue
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
GS110813040013261 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GWGEndoscope, Neurological

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10813040013261]

Hydrogen Peroxide;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-04-15
Device Publish Date2020-04-07

On-Brand Devices [VS3 Iridium ]

10813040013261VS3 Iridium Endoscope-IR 10mm, Long, 0°, Standard FOV - Refurbished
10813040013254VS3 Iridium Endoscope-IR 5.5 mm, 0°, Standard View - Refurbished
10813040013858VS3 Iridium Endoscope-IR 5.5 mm, 0°, Standard View
10813040013636VS3 Iridium Endoscope-IR 10mm, Long, 0°, Standard FOV

Trademark Results [VS3 Iridium]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VS3 IRIDIUM
VS3 IRIDIUM
79170004 4916070 Live/Registered
Visionsense Ltd.
2015-04-19

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