Primary Device ID | 00810052863573 |
NIH Device Record Key | 8ea66ecc-e77c-4283-93ca-7fa2e2fafdb4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Boost 4+ Flex Centrifuge, Dr. PRP |
Version Model Number | 00-389-102-002 |
Catalog Number | 00-389-102-002 |
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 |