Abbott 70901

GUDID 30357599000692

Abbott SF Single Use Lancing Device

ABBOTT DIABETES CARE INC

Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use Glucose monitoring system IVD, home-use
Primary Device ID30357599000692
NIH Device Record Key243021ce-0f42-407f-a2d3-958523fa47b6
Commercial Distribution StatusIn Commercial Distribution
Brand NameAbbott
Version Model Number70901
Catalog Number70901
Company DUNS966390890
Company NameABBOTT DIABETES CARE INC
Device Count200
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 Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx
Phone+1(888)522-5226
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS100357599000691 [Primary]
GS110357599000698 [Unit of Use]
GS130357599000692 [Package]
Contains: 00357599000691
Package: Case [20 Units]
In Commercial Distribution
NDC/NHRIC99073-0709-01 [Secondary]

FDA Product Code

FMKLancet, blood

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-07-16
Device Publish Date2018-06-15

On-Brand Devices [Abbott]

30357599000692Abbott SF Single Use Lancing Device
30699073000843Abbott Diabetes Care USB Data Cable Software
30093815000830Abbott Diabetes Care USB Data Cable Software
30699073709012Abbott SF Single Use Lancing Device
30699073708510Abbott Diabetes Care USB Data Cable Software
30093815708453Abbott Diabetes Care USB Data Cable Software

Trademark Results [Abbott]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ABBOTT
ABBOTT
97705262 not registered Live/Pending
Kimball International, Inc.
2022-12-06
ABBOTT
ABBOTT
90678847 not registered Live/Pending
Nash & Nic, Inc.
2021-04-28
ABBOTT
ABBOTT
90305377 not registered Live/Pending
DELTA FAUCET COMPANY
2020-11-08
ABBOTT
ABBOTT
90283828 not registered Live/Pending
CHEN,Qiong
2020-10-28
ABBOTT
ABBOTT
88470449 not registered Live/Pending
Abbott of England 1981 Ltd.
2019-06-12
ABBOTT
ABBOTT
86892088 not registered Dead/Abandoned
Boutique Hotels, LLC
2016-01-30
ABBOTT
ABBOTT
86726322 5163016 Live/Registered
Nash & Nic, Inc.
2015-08-16
ABBOTT
ABBOTT
77632394 3691666 Dead/Cancelled
Abbott Laboratories
2008-12-12
ABBOTT
ABBOTT
77614503 3741728 Live/Registered
Abbott Laboratories
2008-11-14
ABBOTT
ABBOTT
77614497 4023123 Live/Registered
Abbott Laboratories
2008-11-14
ABBOTT
ABBOTT
77614107 3721018 Dead/Cancelled
Abbott Laboratories
2008-11-13
ABBOTT
ABBOTT
77614103 3724557 Live/Registered
Abbott Laboratories
2008-11-13

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