Primary Device ID | 04053228004394 |
NIH Device Record Key | 69e42746-dd17-40fb-b4bd-37649528c768 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VZV Probe ASR |
Version Model Number | 1 |
Catalog Number | 1067291 |
Company DUNS | 317103745 |
Company Name | QIAGEN GmbH |
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 | false |
Device Combination Product | false |
Single Use | false |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04053228004394 [Primary] |
MVU | Reagents,Specific,Analyte |
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 | 2017-08-15 |
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