Primary Device ID | 04560141946248 |
NIH Device Record Key | 980bb6f3-c8a3-4d1c-8567-7fdf78fb10d9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AeroDR S33/S30 |
Version Model Number | AACU |
Company DUNS | 692076161 |
Company Name | KONICA MINOLTA, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
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 | true |
OTC Over-The-Counter | false |