| Primary Device ID | 10884450014582 |
| NIH Device Record Key | d4d4acfa-d549-4dbc-8e21-5557f44071a0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Slip-Not® |
| Version Model Number | 00884450014585 |
| Catalog Number | SRD200 |
| Company DUNS | 184763290 |
| Company Name | Merit Medical Systems, Inc. |
| 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 | false |
| 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 | 00884450014585 [Primary] |
| GS1 | 10884450014582 [Package] Contains: 00884450014585 Package: [10 Units] In Commercial Distribution |
| GS1 | 20884450014589 [Package] Package: [4 Units] In Commercial Distribution |
| KGS | RETENTION DEVICE, SUTURE |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-04-16 |
| Device Publish Date | 2018-03-16 |
| 10884450014582 | 00884450014585 |
| 10884450014575 | 00884450014578 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SLIP-NOT 86340279 4671875 Live/Registered |
AMERICAN SHORING INC. 2014-07-17 |
![]() SLIP-NOT 77393988 3558803 Live/Registered |
Merit Medical Systems, Inc. 2008-02-11 |
![]() SLIP-NOT 77247499 not registered Dead/Abandoned |
Edel, Margaret R. 2007-08-06 |
![]() SLIP-NOT 73117181 1088010 Dead/Expired |
A. B. CHANCE COMPANY 1977-02-25 |
![]() SLIP-NOT 73025106 1014740 Dead/Cancelled |
ILLINOIS GLOVE COMPANY 1974-06-24 |