Primary Device ID | 00813545021870 |
NIH Device Record Key | c739545a-79bb-4de3-bd14-e29a2e44d867 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ANA R LVR 96 Test |
Version Model Number | 1096L |
Catalog Number | 1096L |
Company DUNS | 155424708 |
Company Name | SCIMEDX CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
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 | 18002215598 |
service@scimedx.com | |
Phone | 18002215598 |
service@scimedx.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00813545021870 [Primary] |
DHN | Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control |
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 | 2016-09-19 |
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