Primary Device ID | 05711781001395 |
NIH Device Record Key | 6f35f073-310b-4f03-bb7f-220520dfaf88 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Entomed By Auditdata |
Version Model Number | SA 203 (Spanish) |
Company DUNS | 310385849 |
Company Name | Auditdata A/S |
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 | false |
Serial Number | true |
Manufacturing Date | true |
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 |