| Primary Device ID | 10884450161958 |
| NIH Device Record Key | f7217df1-613f-4aaa-86ae-b3085c8caec3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SafeSheath CSG |
| Version Model Number | 00884450161951 |
| Catalog Number | FCL-069-00 |
| Company DUNS | 065673912 |
| Company Name | Merit Medical |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| 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 | 00884450161951 [Primary] |
| GS1 | 10884450161958 [Package] Contains: 00884450161951 Package: [5 Units] In Commercial Distribution |
| DYB | INTRODUCER, CATHETER |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-06-07 |
| Device Publish Date | 2017-02-20 |
| 10884450162108 | 00884450162101 |
| 10884450162061 | 00884450162064 |
| 10884450162054 | 00884450162057 |
| 10884450162047 | 00884450162040 |
| 10884450162030 | 00884450162033 |
| 10884450162009 | 00884450162002 |
| 10884450161996 | 00884450161999 |
| 10884450161989 | 00884450161982 |
| 10884450161972 | 00884450161975 |
| 10884450161958 | 00884450161951 |
| 10884450161941 | 00884450161944 |