| Primary Device ID | 10801741012461 |
| NIH Device Record Key | bd588121-1780-49ed-bd87-1042f31dee1e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Catheter Repair Kit |
| Version Model Number | 5581000 |
| Catalog Number | 5581000 |
| Company DUNS | 044611812 |
| Company Name | Bard Access Systems, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00801741012464 [Primary] |
| GS1 | 10801741012461 [Package] Contains: 00801741012464 Package: CA [5 Units] In Commercial Distribution |
| GS1 | 20801741012468 [Package] Package: BX [60 Units] In Commercial Distribution |
| MSD | Catheter, hemodialysis, implanted |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2015-05-06 |
| 20801741045107 | Catheter Repair Kit |
| 10801741045087 | Catheter Repair Kit with Replacement Connector |
| 10801741012461 | DUET CATHETER REPAIR KIT |