Primary Device ID | 00365702544109 |
NIH Device Record Key | 766c1b39-d4bf-4d56-9b71-83ddbba58d56 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ACCU-CHEK AVIVA |
Version Model Number | 06870287001 |
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 | true |
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 | 00365702544109 [Primary] |
LFR | Glucose Dehydrogenase, Glucose |
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 |
00365702725102 | ACCU-CHEK AVIVA PLUS METER ONLY US |
10365702724102 | ACCU-CHEK AVIVA PLUS SAMPLE KIT 20/CASE |
00365702723108 | Accu-Chek Aviva Plus Retail Kit 10/case |
00365702544109 | ACCU-CHEK AVIVA MG/DL 455 US |
00365702107106 | ACCU-CHEK AVIVA 2 LEVEL CONTROL 6/CS |
00365702702394 | ACCU-CHEK AVIVA MG/DL 455 US NON-VA |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ACCU-CHEK AVIVA 78343530 3071846 Live/Registered |
Roche Diagnostics GmbH 2003-12-19 |