ACCU-CHEK AVIVA PLUS 06988601001

GUDID 00365702102101

ACCU-CHEK AVIVA PLUS METER-ONLY

Roche Diagnostics Operations, Inc.

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Primary Device ID00365702102101
NIH Device Record Keyefad36f1-438f-43b8-ad51-d4b7b7437843
Commercial Distribution Discontinuation2018-08-29
Commercial Distribution StatusNot in Commercial Distribution
Brand NameACCU-CHEK AVIVA PLUS
Version Model Number06988601001
Catalog Number06988601001
Company DUNS141608724
Company NameRoche Diagnostics Operations, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100365702102101 [Primary]
GS110365702102108 [Package]
Package: [12 Units]
Discontinued: 2018-08-29
Not in Commercial Distribution

FDA Product Code

NBWSystem, Test, Blood Glucose, Over The Counter

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-04-29
Device Publish Date2016-08-26

On-Brand Devices [ACCU-CHEK AVIVA PLUS ]

00365702700932VIAL LBLD 10CT STRIP AC AVIVA PLUS BRK
00365702445109ACCU-CHEK AVIVA PLUS SAMPLE KIT 16/CASE
10365702438108ACCU-CHEK AVIVA PLUS 50 HN STP BRK 36/CS
00365702437104ACCU-CHEK AVIVA PLUS 50 MED-BEN BRK 36/C
10365702436104ACCU-CHEK AVIVA PLUS 50 MLRDR BRK 36/CS
10365702408101ACCU-CHEK AVIVA PLUS 100CT STRP BRK 24/C
10365702407104ACCU-CHEK AVIVA PLUS 50CT STRIP BRK 36/C
00365702405103ACCU-CHEK AVIVA PLUS 10CT STRIP BRK
00365702134102ACCU-CHEK AVIVA PLUS HNP KIT 8/CASE
00365702102101ACCU-CHEK AVIVA PLUS METER-ONLY
00365702101104ACCU-CHEK AVIVA PLUS RETAIL KIT 8/CASE

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