Primary Device ID | 10365702578101 |
NIH Device Record Key | ee703dd2-c2af-46c8-90d6-e7433274cf6d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ACCU-CHEK AVIVA CONNECT |
Version Model Number | 07049811001 |
Catalog Number | 07049811001 |
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 | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | true |
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 | 00365702578104 [Primary] |
GS1 | 10365702578101 [Package] Contains: 00365702578104 Package: [8 Units] In Commercial Distribution |
NBW | System, Test, Blood Glucose, Over The Counter |
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 | 2016-08-26 |
00365702593107 | ACCU-CHEK AVIVA CONNECT MG/DL (502) |
10365702578101 | ACCU-CHEK AVIVA CONNECT MG/DL M-O |
10365702577104 | ACCU-CHEK AVIVA CONNECT RETAIL KIT 8/CASE |
10365702576107 | ACCU-CHEK AVIVA CONNECT SAMPLE KIT 16/CASE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ACCU-CHEK AVIVA CONNECT 79133250 4561864 Live/Registered |
Roche Diabetes Care GmbH 2013-05-06 |