Primary Device ID | 10815845020024 |
NIH Device Record Key | a254ae47-2aff-4040-a012-d7d298001fe1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Clearview® |
Version Model Number | 92002 |
Company DUNS | 194854949 |
Company Name | ALERE SAN DIEGO, INC. |
Device Count | 30 |
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 | 00815845020027 [Unit of Use] |
GS1 | 10815845020024 [Primary] |
GTY | Antigens, All Groups, Streptococcus Spp. |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2022-06-10 |
Device Publish Date | 2016-09-24 |
10815845020024 | 92002 |
10815845020000 | 92401 |
10815845020048 | 92405 |