ColoScreen-ES Developer-15

GUDID M52550881

HELENA LABORATORIES CORPORATION

Faecal occult blood IVD, kit, rapid colorimetric, clinical
Primary Device IDM52550881
NIH Device Record Keycdbaf8a5-768f-4adb-84f1-b8ee47b33aac
Commercial Distribution StatusIn Commercial Distribution
Brand NameColoScreen-ES Developer-15
Version Model Number5088
Company DUNS079396131
Company NameHELENA LABORATORIES CORPORATION
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
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

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM52550880 [Primary]
HIBCCM52550881 [Package]
Contains: M52550880
Package: Box [20 Units]
In Commercial Distribution

FDA Product Code

KHEREAGENT, OCCULT BLOOD

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2022-11-28
Device Publish Date2016-08-18

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M52594200 - IFE IgE Antiserum2024-10-07
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M52518360 - V8 Urine Preparation Buffer2023-09-18
M5255526930 - SPIFE Nexus Split Beta SPE - 80, 100 Gel Kit2023-09-18
M52510680010 - SPIFE Touch, CSA 2015 (120V)2023-09-11

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