Primary Device ID | 00697077000974 |
NIH Device Record Key | 7518032b-8296-450e-beb5-076f52a883cb |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | CRB-LF10K-1KF |
Company DUNS | 203163290 |
Company Name | Amico Diagnostic Incorporated |
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 | true |
OTC Over-The-Counter | false |