Primary Device ID | 00841785113444 |
NIH Device Record Key | 027fd09b-5ec0-4f1c-b8c3-4cb5d2e4c2d6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Symmetry Surgical |
Version Model Number | e2401-51 |
Catalog Number | e2401-51 |
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 | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841785113444 [Primary] |
GBZ | Catheter, Cholangiography |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-10-03 |
Device Publish Date | 2019-09-25 |
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 |