Primary Device ID | 10842430105866 |
NIH Device Record Key | 0c44c4d8-14c6-4677-ab21-64d1eb056687 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SUPINE / LATERAL HEAD REST |
Version Model Number | 1902 |
Catalog Number | 1902-20 |
Company DUNS | 084527241 |
Company Name | MIZUHO ORTHOPEDIC SYSTEMS, INC. |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |