Primary Device ID | 00887482128411 |
NIH Device Record Key | d3a205cf-e45c-4122-9482-5cbab403df69 |
Commercial Distribution Discontinuation | 9999-01-01 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Symmetry Surgical SMITH-PETERSON |
Version Model Number | 88-1009 |
Catalog Number | 88-1009 |
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 |
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