Primary Device ID | 00887482139479 |
NIH Device Record Key | 2f143dbf-0e0c-45c9-9501-c2e8671b474b |
Commercial Distribution Discontinuation | 9999-01-01 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Symmetry Rhoton® Scoville-Greenwood |
Version Model Number | 08-0033 |
Catalog Number | 08-0033 |
Company DUNS | 079641356 |
Company Name | SYMMETRY SURGICAL INC. |
Device Count | 1 |
DM Exempt | true |
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 | true |
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 |