Primary Device ID | 00810052864310 |
NIH Device Record Key | 16ffe6ea-a111-490e-a724-6050ae839265 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Horizon 6 Flex FA (DC) Centrifuge, Drucker |
Version Model Number | 00-376-009-007 |
Catalog Number | 00-376-009-007 |
Company DUNS | 022156957 |
Company Name | DRUCKER DIAGNOSTICS |
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 | true |
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 |
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