| 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 |