Primary Device ID | 07640137341596 |
NIH Device Record Key | 8c2c0a7f-924e-4ebd-9107-92e583b1cb04 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Search-Cyte Pool 0.8% |
Version Model Number | 3x10 ml |
Catalog Number | 213289 |
Company DUNS | 483287020 |
Company Name | Medion Grifols Diagnostics AG |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Device Kit | true |
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 | false |
OTC Over-The-Counter | false |