| Primary Device ID | 00855208005049 |
| NIH Device Record Key | 4cc23afe-6e1e-43d2-820b-f15be03a17b2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BNX |
| Version Model Number | DSN-25-02 |
| Catalog Number | DSN-25-02 |
| Company DUNS | 058614483 |
| Company Name | Covidien LP |
| 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 | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Special Storage Condition, Specify | Between 0 and 0 *; |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00855208005049 [Primary] |
| FCG | Biopsy needle |
| 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 | 2016-09-24 |
| 00855208005070 | FINE NEEDLE ASPIRATION NEEDLE |
| 00855208005063 | FINE NEEDLE ASPIRATION NEEDLE |
| 00855208005056 | FINE NEEDLE ASPIRATION NEEDLE |
| 00855208005049 | FINE NEEDLE ASPIRATION SYSTEM |
| 00855208005032 | FINE NEEDLE ASPIRATION SYSTEM |
| 00855208005025 | FINE NEEDLE ASPIRATION SYSTEM |
| 00855208005018 | FINE NEEDLE ASPIRATION SYSTEM |
| 00855208005001 | FINE NEEDLE ASPIRATION SYSTEM |