| Primary Device ID | 50382903817035 |
| NIH Device Record Key | 5a7132aa-060b-44a7-995b-ccac01d81030 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BD Angiocath Autoguard |
| Version Model Number | 381703 |
| Catalog Number | 381703 |
| Company DUNS | 124987988 |
| Company Name | BECTON, DICKINSON AND COMPANY |
| Device Count | 50 |
| DM Exempt | true |
| 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 | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00382903817030 [Unit of Use] |
| GS1 | 30382903817031 [Primary] |
| GS1 | 50382903817035 [Package] Contains: 30382903817031 Package: Case [4 Units] In Commercial Distribution |
| FOZ | Catheter,intravascular,therapeutic,short-term less than 30 days |
| 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 | 2016-09-16 |
| 50382903817097 | ANGIOCATH AUTOGUARD ORN 14GA X 1.75IN |
| 50382903817080 | ANGIOCATH AUTOGUARD GRAY 16GA X 1.77IN |
| 50382903817073 | ANGIOCATH AUTOGUARD GRAY 16GA X 1.16IN |
| 50382903817066 | ANGIOCATH AUTOGUARD GN 18GA X 1.88IN |
| 50382903817059 | ANGIOCATH AUTOGUARD GN 18GA X 1.16IN |
| 50382903817042 | ANGIOCATH AUTOGUARD PNK 20GA X 1.88IN |
| 50382903817035 | ANGIOCATH AUTOGUARD PNK 20GA X 1.16IN |
| 50382903817028 | ANGIOCATH AUTOGUARD PNK 20GA X 1.0IN |
| 50382903817011 | ANGIOCATH AUTOGUARD BLU 22GA X 1.0IN |
| 50382903817004 | ANGIOCATH AUTOGUARD YEL 24GA X .75IN |