ESH Touch (120/230V)

GUDID M52513800000

HELENA LABORATORIES CORPORATION

Pipetting system IVD Pipetting system IVD Pipetting system IVD Pipetting system IVD Pipetting system IVD Pipetting system IVD Pipetting system IVD Pipetting system IVD Pipetting system IVD Pipetting system IVD Pipetting system IVD Pipetting system IVD Pipetting system IVD Pipetting system IVD Pipetting system IVD Pipetting system IVD Pipetting system IVD Pipetting system IVD
Primary Device IDM52513800000
NIH Device Record Keya5fa6e7b-17ab-4068-a6f3-dcda06fc79e5
Commercial Distribution StatusIn Commercial Distribution
Brand NameESH Touch (120/230V)
Version Model Number1380000
Company DUNS836287433
Company NameHELENA LABORATORIES CORPORATION
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)231-5663
Emailhelena@helena.com
Phone+1(800)231-5663
Emailhelena@helena.com
Phone+1(800)231-5663
Emailhelena@helena.com
Phone+1(800)231-5663
Emailhelena@helena.com
Phone+1(800)231-5663
Emailhelena@helena.com
Phone+1(800)231-5663
Emailhelena@helena.com
Phone+1(800)231-5663
Emailhelena@helena.com
Phone+1(800)231-5663
Emailhelena@helena.com
Phone+1(800)231-5663
Emailhelena@helena.com
Phone+1(800)231-5663
Emailhelena@helena.com
Phone+1(800)231-5663
Emailhelena@helena.com
Phone+1(800)231-5663
Emailhelena@helena.com
Phone+1(800)231-5663
Emailhelena@helena.com
Phone+1(800)231-5663
Emailhelena@helena.com
Phone+1(800)231-5663
Emailhelena@helena.com
Phone+1(800)231-5663
Emailhelena@helena.com
Phone+1(800)231-5663
Emailhelena@helena.com
Phone+1(800)231-5663
Emailhelena@helena.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM52513800000 [Primary]

FDA Product Code

JQWSTATION, PIPETTING AND DILUTING, FOR CLINICAL USE

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2023-09-11
Device Publish Date2017-03-17

Devices Manufactured by HELENA LABORATORIES CORPORATION

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M52510690000 - SPIFE Touch (230V)2023-09-11
M52510880010 - SPIFE 3000 w/ New Pump & Valve (110V)2023-09-11
M52510880020 - SPIFE 3000, "CE 2011" (120V)2023-09-11
M52510890010 - SPIFE 3000 w/ New Pump & Valve (220V)2023-09-11
M52510890020 - SPIFE 3000, "CE 2011" (230V)2023-09-11

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