SLS 2500

GUDID 00815871020619

Avante

Operating light system
Primary Device ID00815871020619
NIH Device Record Key49aeb396-dc23-4cab-ad65-b11107768975
Commercial Distribution StatusIn Commercial Distribution
Brand NameSLS 2500
Version Model Number70Z260MD
Company DUNS178440426
Company NameAvante
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100815871020619 [Primary]

FDA Product Code

FQPLamp, Operating-Room

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-06-19
Device Publish Date2016-09-23

On-Brand Devices [SLS 2500]

0081587102148770Z260D
0081587102064070Z260SL-9
0081587102063370Z260SLW
0081587102062670Z260SL
0081587102061970Z260MD
0081587102060270Z260M

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