| Primary Device ID | 20802526563229 |
| NIH Device Record Key | 47f2065c-3626-4b57-b74a-64601447109d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LIGATURE SLEEVE |
| Version Model Number | 664760-302 |
| Catalog Number | LS21-10 |
| Company DUNS | 101835833 |
| Company Name | Oscor Inc. |
| Device Count | 10 |
| DM Exempt | false |
| 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 | 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 | 00802526563225 [Unit of Use] |
| GS1 | 20802526563229 [Primary] |
| DTB | Permanent Pacemaker Electrode |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-07-07 |
| 70836559007424 | LS17B20 |
| 70836559002023 | LS26B20 |
| 70836559002016 | LS24B20 |
| 70836559002009 | LS21B20 |
| 70836559001996 | LS18B20 |
| 70836559001989 | LS15B20 |
| 20885672008349 | Ligature Sleeve |
| 20802526563229 | 664760-302 |
| 00836559007425 | LS-17 |
| 00836559002024 | LS-26 |
| 00836559002017 | LS-24 |
| 00836559002000 | LS-21 |
| 00836559001997 | LS-18 |
| 00836559001980 | LS-15 |