| Primary Device ID | EHKM10023531 |
| NIH Device Record Key | bc74376f-f6de-43b7-b0bf-8608be434e6f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CliP Partial FlexiBAL Titanium |
| Version Model Number | 1002353 |
| Catalog Number | 1002353 |
| 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 | EHKM10023531 [Primary] |
| ETB | Prosthesis, Partial Ossicular Replacement |
| 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 |
| EHKM10023571 | Ossicular Prosthesis, partial |
| EHKM10023561 | Ossicular Prosthesis, partial |
| EHKM10023551 | Ossicular Prosthesis, partial |
| EHKM10023541 | Ossicular Prosthesis, partial |
| EHKM10023531 | Ossicular Prosthesis, partial |
| EHKM10023521 | Ossicular Prosthesis, partial |
| EHKM10023511 | Ossicular Prosthesis, partial |
| EHKM10023501 | Ossicular Prosthesis, partial |
| EHKM10023681 | Ossicular Prosthesis, partial |
| EHKM10023661 | Ossicular Prosthesis, partial |
| EHKM10023641 | Ossicular Prosthesis, partial |