Primary Device ID | 00365702101104 |
NIH Device Record Key | 0189dace-477f-4269-a95a-e651386cb10e |
Commercial Distribution Discontinuation | 2018-07-19 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | ACCU-CHEK AVIVA PLUS |
Version Model Number | 06988580001 |
Catalog Number | 06988580001 |
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 | 00365702101104 [Primary] |
GS1 | 10365702101101 [Package] Package: [8 Units] Discontinued: 2018-07-19 Not 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 | 3 |
Public Version Date | 2019-04-29 |
Device Publish Date | 2016-08-26 |
00365702700932 | VIAL LBLD 10CT STRIP AC AVIVA PLUS BRK |
00365702445109 | ACCU-CHEK AVIVA PLUS SAMPLE KIT 16/CASE |
10365702438108 | ACCU-CHEK AVIVA PLUS 50 HN STP BRK 36/CS |
00365702437104 | ACCU-CHEK AVIVA PLUS 50 MED-BEN BRK 36/C |
10365702436104 | ACCU-CHEK AVIVA PLUS 50 MLRDR BRK 36/CS |
10365702408101 | ACCU-CHEK AVIVA PLUS 100CT STRP BRK 24/C |
10365702407104 | ACCU-CHEK AVIVA PLUS 50CT STRIP BRK 36/C |
00365702405103 | ACCU-CHEK AVIVA PLUS 10CT STRIP BRK |
00365702134102 | ACCU-CHEK AVIVA PLUS HNP KIT 8/CASE |
00365702102101 | ACCU-CHEK AVIVA PLUS METER-ONLY |
00365702101104 | ACCU-CHEK AVIVA PLUS RETAIL KIT 8/CASE |