ClearCRIT® Plastic Capillary Tubes 270-106

GUDID 00831829000267

SEPARATION TECHNOLOGY, INC.

Capillary blood collection tube IVD, ammonium heparin
Primary Device ID00831829000267
NIH Device Record Key0d03bd2c-3aec-44f5-9d3c-06ba153b26a4
Commercial Distribution StatusIn Commercial Distribution
Brand NameClearCRIT® Plastic Capillary Tubes
Version Model Number270-106
Catalog Number270-106
Company DUNS195501127
Company NameSEPARATION TECHNOLOGY, INC.
Device Count5
DM Exemptfalse
Pre-market Exempttrue
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

Phone18005315535
Emailstanbiolab@ekfdiagnostics.com

Operating and Storage Conditions

Storage Environment TemperatureBetween 15 Degrees Celsius and 30 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100831829000267 [Primary]
GS100831829000274 [Unit of Use]

FDA Product Code

GIOTube, Collection, Capillary Blood

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-08-09
Device Publish Date2017-08-25

On-Brand Devices [ClearCRIT® Plastic Capillary Tubes]

00831829000281270-107
00831829000267270-106

Trademark Results [ClearCRIT]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CLEARCRIT
CLEARCRIT
76114293 2487367 Live/Registered
SEPARATION TECHNOLOGY, INC.
2000-08-22

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