Leica Biosystems Ariol SL200 Stage

GUDID 00849832011606

Leica Biosystems Ariol SL200 Stage

Leica Biosystems Richmond, Inc.

Cell morphology analyser IVD, automated
Primary Device ID00849832011606
NIH Device Record Key302984b0-f054-4afe-a750-3c47b6ef7f7c
Commercial Distribution StatusIn Commercial Distribution
Brand NameLeica Biosystems Ariol SL200 Stage
Version Model Number23ASLSTAGE
Company DUNS082930884
Company NameLeica Biosystems Richmond, Inc.
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 Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(866)4783999
Emailtech.support@Leicabiosystems.com
Phone+1(866)4783999
Emailtech.support@Leicabiosystems.com
Phone+1(866)4783999
Emailtech.support@Leicabiosystems.com
Phone+1(866)4783999
Emailtech.support@Leicabiosystems.com
Phone+1(866)4783999
Emailtech.support@Leicabiosystems.com
Phone+1(866)4783999
Emailtech.support@Leicabiosystems.com
Phone+1(866)4783999
Emailtech.support@Leicabiosystems.com
Phone+1(866)4783999
Emailtech.support@Leicabiosystems.com
Phone+1(866)4783999
Emailtech.support@Leicabiosystems.com
Phone+1(866)4783999
Emailtech.support@Leicabiosystems.com
Phone+1(866)4783999
Emailtech.support@Leicabiosystems.com
Phone+1(866)4783999
Emailtech.support@Leicabiosystems.com
Phone+1(866)4783999
Emailtech.support@Leicabiosystems.com
Phone+1(866)4783999
Emailtech.support@Leicabiosystems.com
Phone+1(866)4783999
Emailtech.support@Leicabiosystems.com

Device Dimensions

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Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *
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Special Storage Condition, SpecifyBetween 0 and 0 *
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Device Identifiers

Device Issuing AgencyDevice ID
GS100849832011606 [Primary]

FDA Product Code

NQNMICROSCOPE,AUTOMATED,IMAGE ANALYSIS,IMMUNOHISTOCHEMISTRY,OPERATOR INTERVENTION,NUCLEAR INTENSITY & PERCENT POSITIVITY

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-04-21

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