Primary Device ID | 00365702700017 |
NIH Device Record Key | 1ac106ee-9805-471a-8420-65eba124c1a9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ACCU-CHEK CONNECT |
Version Model Number | 07250452001 |
Company DUNS | 141608724 |
Company Name | Roche Diagnostics Operations, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00365702700017 [Primary] |
NDC | Calculator, Drug Dose |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-13 |
00365702700017 | ACCU-CHEK CONNECT DIABETES MANAGEMENT AP |
00365702700000 | ACCU-CHEK CONNECT DIABETES MGMT iAP |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ACCU-CHEK CONNECT 86185145 4846710 Live/Registered |
Roche Diabetes Care GmbH 2014-02-05 |
ACCU-CHEK CONNECT 86185123 4592941 Live/Registered |
Roche Diagnostics GmbH 2014-02-05 |
ACCU-CHEK CONNECT 85537318 not registered Dead/Abandoned |
Roche Diagnostics GmbH 2012-02-08 |