| Primary Device ID | EHKM10040341 |
| NIH Device Record Key | 7895f8ae-79f5-49ca-ba8e-7b210acf8407 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Duesseldorf Type AERIAL Total Titanium |
| Version Model Number | 1004034 |
| Catalog Number | 1004034 |
| Company DUNS | 341155720 |
| Company Name | Heinz Kurz GmbH |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 |
| Phone | +49707291790 |
| info@kurzmed.com |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | EHKM10040341 [Primary] |
| ETA | Replacement, Ossicular Prosthesis, Total |
| 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 | 2015-09-21 |
| EHKM10040491 | Ossicular Prosthesis, total |
| EHKM10040481 | Ossicular Prosthesis, total |
| EHKM10040461 | Ossicular Prosthesis, total |
| EHKM10040441 | Ossicular Prosthesis, total |
| EHKM10040431 | Ossicular Prosthesis, total |
| EHKM10040421 | Ossicular Prosthesis, total |
| EHKM10040411 | Ossicular Prosthesis, total |
| EHKM10040401 | Ossicular Prosthesis, total |
| EHKM10040391 | Ossicular Prosthesis, total |
| EHKM10040381 | Ossicular Prosthesis, total |
| EHKM10040371 | Ossicular Prosthesis, total |
| EHKM10040361 | Ossicular Prosthesis, total |
| EHKM10040351 | Ossicular Prosthesis, total |
| EHKM10040341 | Ossicular Prosthesis, total |