Primary Device ID | 10845717000489 |
NIH Device Record Key | 60c99602-2f2f-4f1f-b46c-ca010ac0464a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VERIDIAN |
Version Model Number | 02-12702 |
Company DUNS | 830437997 |
Company Name | VERIDIAN HEALTHCARE LLC |
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 | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 866-326-1313 |
info@veridianhealthcare.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00845717000482 [Primary] |
GS1 | 10845717000489 [Package] Contains: 00845717000482 Package: MASTER CARTON [20 Units] In Commercial Distribution |
DXN | System, Measurement, Blood-Pressure, Non-Invasive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-26 |
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