| Primary Device ID | 00887482140772 |
| NIH Device Record Key | f78e7d3a-b562-40db-aa1a-1a6b1de9d11d |
| Commercial Distribution Discontinuation | 9999-01-01 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Symmetry Rhoton® Ultra |
| Version Model Number | 08-0317 |
| Catalog Number | 08-0317 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887482140772 [Primary] |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00887482140772]
Moist Heat or Steam Sterilization
[00887482140772]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-05-31 |
| 00887482140772 | Forcep Bipolar 8 5/8In 1mm Bayonet Curved Down Instruments |
| 00887482140758 | Forcep Bipolar 7 3/4In 1Mm Bayonet Curved Up Instruments |
| 00887482140741 | Forcep Bipolar 7 3/4In 1mm Bayonet Curved Down Instruments |
| 00887482140734 | Forcep Bipolar 1mm Bayonet Instruments |