| Primary Device ID | 50382903817202 |
| NIH Device Record Key | 37fa8169-3fe9-4e50-b816-a1de5970847c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BD Angiocath-N Autoguard |
| Version Model Number | 381720 |
| Catalog Number | 381720 |
| 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 | 00382903817207 [Unit of Use] |
| GS1 | 30382903817208 [Primary] |
| GS1 | 50382903817202 [Package] Contains: 30382903817208 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 |
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| 60382904455707 - BD BACTEC™ 9120 | 2024-11-12 BD BACTEC™ 9120 |
| 00382904458003 - BD BACTEC™ 9050 | 2024-11-11 BD BACTEC™ 9050 |
| 00382904454166 - BD Onclarity HPV Self Collection Diluent Tube | 2024-11-11 BD Onclarity HPV Self Collection Diluent Tube |
| 00382906639844 - Horizon | 2024-10-22 CD138 (MI15) BV421 ASR |
| 00382906651204 - Horizon | 2024-10-22 CD197 (2-L1-A) APC-R700 ASR |
| 00382906651297 - Horizon | 2024-10-22 CD194 (1G1) BV421 ASR |
| 00382906651334 - Horizon | 2024-10-22 CD40 (5C3) BV605 ASR |