Primary Device ID | 00887482076866 |
NIH Device Record Key | 57a3048d-7827-47b2-af32-d1b66b96194f |
Commercial Distribution Discontinuation | 9999-01-01 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Symmetry Cohen |
Version Model Number | 52-0839 |
Catalog Number | 52-0839 |
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 | false |
OTC Over-The-Counter | false |
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