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 |