| Primary Device ID | 30841785113384 |
| NIH Device Record Key | e4680693-afcd-4ecc-b237-4408cdbf5f8e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Symmetry Surgical |
| Version Model Number | e2504-01 |
| Catalog Number | e2504-01 |
| Company DUNS | 079344210 |
| Company Name | OLSEN MEDICAL, LLC |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00841785113383 [Primary] |
| GS1 | 30841785113384 [Package] Contains: 00841785113383 Package: [4 Units] In Commercial Distribution |
| GAD | Retractor |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-08-21 |
| Device Publish Date | 2019-07-02 |
| 30841785113384 | e2504-01 |
| 00841785113468 | e2401-53 |
| 00841785113451 | e2401-52 |
| 00841785113444 | e2401-51 |
| 00841785113437 | e2401-50 |
| 00841785113420 | e2400-53 |
| 00841785113413 | e2400-52 |
| 00841785113406 | e2400-51 |
| 00841785113390 | e2400-50 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SYMMETRY SURGICAL 85528900 4407791 Live/Registered |
SPECIALTY SURGICAL INSTRUMENTATION, INC. 2012-01-30 |
![]() SYMMETRY SURGICAL 85526378 4404038 Live/Registered |
SPECIALTY SURGICAL INSTRUMENTATION, INC. 2012-01-26 |
![]() SYMMETRY SURGICAL 85526317 4404037 Live/Registered |
SPECIALTY SURGICAL INSTRUMENTATION, INC. 2012-01-26 |