EasyPoint® 26011

GUDID 00613703260116

22G x 1 1/4" EasyPoint® Blood Collection Tube Holder with Needle

RETRACTABLE TECHNOLOGIES, INC.

Blood collection tube holder/needle
Primary Device ID00613703260116
NIH Device Record Key8a2f2d4b-860b-4ebc-b9e0-7592247e39f8
Commercial Distribution StatusIn Commercial Distribution
Brand NameEasyPoint®
Version Model Number26011
Catalog Number26011
Company DUNS838024255
Company NameRETRACTABLE TECHNOLOGIES, 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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone972-294-1010
Emailrtiservice@retractable.com
Phone972-294-1010
Emailrtiservice@retractable.com
Phone972-294-1010
Emailrtiservice@retractable.com
Phone972-294-1010
Emailrtiservice@retractable.com
Phone972-294-1010
Emailrtiservice@retractable.com
Phone972-294-1010
Emailrtiservice@retractable.com
Phone972-294-1010
Emailrtiservice@retractable.com
Phone972-294-1010
Emailrtiservice@retractable.com
Phone972-294-1010
Emailrtiservice@retractable.com
Phone972-294-1010
Emailrtiservice@retractable.com
Phone972-294-1010
Emailrtiservice@retractable.com
Phone972-294-1010
Emailrtiservice@retractable.com
Phone972-294-1010
Emailrtiservice@retractable.com
Phone972-294-1010
Emailrtiservice@retractable.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100613703260109 [Primary]
GS100613703260116 [Package]
Contains: 00613703260109
Package: Case [100 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JKATubes, Vials, Systems, Serum Separators, Blood Collection

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-04-26
Device Publish Date2023-04-18

On-Brand Devices [EasyPoint®]

0061370382092125G x 5/8" EasyPoint® Needle
0061370382032723G x 1" EasyPoint® Needle
0061370382012925G x 1" EasyPoint® Needle
0061370385291525G x 5/8" EasyPoint® Needle
0061370385231123G x 1" EasyPoint® Needle
0061370385211325G x 1" EasyPoint® Needle
0061370385091118G x 1 1/2" EasyPoint® Needle
0061370385081218G x 1" EasyPoint® Needle
0061370385071320G x 1 1/2" EasyPoint® Needle
0061370385061420G x 1" EasyPoint® Needle
0061370385051521G x 1 1/2" EasyPoint® Needle
0061370385041621G x 1" EasyPoint® Needle
0061370385031722G x 1 1/2" EasyPoint® Needle
0061370385021822G x 1" EasyPoint® Needle
0061370385011925G x 1 1/2" EasyPoint® Needle
0061370382211630G x 1/2" EasyPoint® Needle
0061370326021521G x 1 1/4" EasyPoint® Blood Collection Tube Holder with Needle
0061370326011622G x 1 1/4" EasyPoint® Blood Collection Tube Holder with Needle

Trademark Results [EasyPoint]

Mark Image

Registration | Serial
Company
Trademark
Application Date
EASYPOINT
EASYPOINT
98599263 not registered Live/Pending
Retractable Technologies, Inc.
2024-06-13
EASYPOINT
EASYPOINT
90852936 not registered Live/Pending
Retractable Technologies, Inc.
2021-07-28
EASYPOINT
EASYPOINT
86052912 5008428 Live/Registered
Retractable Technologies, Inc.
2013-08-30
EASYPOINT
EASYPOINT
79073486 3825321 Dead/Cancelled
austriamicrosystems AG
2009-08-11
EASYPOINT
EASYPOINT
78104007 not registered Dead/Abandoned
NCR Corporation
2002-01-22
EASYPOINT
EASYPOINT
78031579 2735569 Dead/Cancelled
NCR Corporation
2000-10-20
EASYPOINT
EASYPOINT
74467240 1924599 Dead/Cancelled
Flagship Group II, Inc., The
1993-12-08

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.