| Primary Device ID | 04250676708861 |
| NIH Device Record Key | 6bdb840e-f58b-4b22-80e6-cf8ab3e632b3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Brünings septal forceps |
| Version Model Number | 25-100-02 |
| Catalog Number | 25-100-02 |
| Company DUNS | 332893028 |
| Company Name | Spiggle & Theis Medizintechnik GmbH |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |