Primary Device ID | 10815845020017 |
NIH Device Record Key | aad11dfc-59a8-46ba-a809-5c16990185c3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Acceava® |
Version Model Number | 92404 |
Company DUNS | 194854949 |
Company Name | ALERE SAN DIEGO, INC. |
Device Count | 25 |
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 | true |
Lot Batch | true |
Serial Number | false |
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 |
Phone | 866-216-0094 |
xx@xx.xx | |
Phone | 866-216-0094 |
xx@xx.xx | |
Phone | 866-216-0094 |
xx@xx.xx | |
Phone | 866-216-0094 |
xx@xx.xx | |
Phone | 866-216-0094 |
xx@xx.xx | |
Phone | 866-216-0094 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00815845020010 [Unit of Use] |
GS1 | 10815845020017 [Primary] |
KTN | System, Test, Infectious Mononucleosis |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2022-06-10 |
Device Publish Date | 2016-09-24 |
10815845020031 | 92001 |
10815845020017 | 92404 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ACCEAVA 75308530 2241201 Live/Registered |
ALERE SAN DIEGO, INC. 1997-06-13 |
ACCEAVA 75308336 2241963 Live/Registered |
ALERE SAN DIEGO, INC. 1997-06-13 |