Primary Device ID | 30093815000830 |
NIH Device Record Key | 000b46f0-e616-4bd1-85bc-e05c564809a8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Abbott |
Version Model Number | 70845 |
Catalog Number | 70845 |
Company DUNS | 966390890 |
Company Name | ABBOTT DIABETES CARE INC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx | |
Phone | +1(888)522-5226 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00093815000839 [Primary] |
GS1 | 30093815000830 [Package] Contains: 00093815000839 Package: Case [40 Units] In Commercial Distribution |
NDC/NHRIC | 57599-0845-1 [Secondary] |
OUG | Medical device data system |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-04-02 |
Device Publish Date | 2018-02-28 |
30357599000692 | Abbott SF Single Use Lancing Device |
30699073000843 | Abbott Diabetes Care USB Data Cable Software |
30093815000830 | Abbott Diabetes Care USB Data Cable Software |
30699073709012 | Abbott SF Single Use Lancing Device |
30699073708510 | Abbott Diabetes Care USB Data Cable Software |
30093815708453 | Abbott Diabetes Care USB Data Cable Software |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ABBOTT 97705262 not registered Live/Pending |
Kimball International, Inc. 2022-12-06 |
ABBOTT 90678847 not registered Live/Pending |
Nash & Nic, Inc. 2021-04-28 |
ABBOTT 90305377 not registered Live/Pending |
DELTA FAUCET COMPANY 2020-11-08 |
ABBOTT 90283828 not registered Live/Pending |
CHEN,Qiong 2020-10-28 |
ABBOTT 88470449 not registered Live/Pending |
Abbott of England 1981 Ltd. 2019-06-12 |
ABBOTT 86892088 not registered Dead/Abandoned |
Boutique Hotels, LLC 2016-01-30 |
ABBOTT 86726322 5163016 Live/Registered |
Nash & Nic, Inc. 2015-08-16 |
ABBOTT 77632394 3691666 Dead/Cancelled |
Abbott Laboratories 2008-12-12 |
ABBOTT 77614503 3741728 Live/Registered |
Abbott Laboratories 2008-11-14 |
ABBOTT 77614497 4023123 Live/Registered |
Abbott Laboratories 2008-11-14 |
ABBOTT 77614107 3721018 Dead/Cancelled |
Abbott Laboratories 2008-11-13 |
ABBOTT 77614103 3724557 Live/Registered |
Abbott Laboratories 2008-11-13 |