| Primary Device ID | 04050052026967 |
| NIH Device Record Key | d56cabf6-4a9c-470b-b5c5-32a74e69de0f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | N/A |
| Version Model Number | 710001 |
| Catalog Number | 710001 |
| Company DUNS | 315919220 |
| Company Name | Eberle GmbH & Co. KG |
| 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 | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04050052026967 [Primary] |
| LHX | Trousers, anti-shock |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-05-28 |
| Device Publish Date | 2018-04-27 |
| 04050052031015 - EBERLE | 2018-07-31 Full Radius Resector Sharp Cut 4,2 |
| 04050052030902 - EBERLE | 2018-07-31 Aggressive Full Radius Resector 4,2 |
| 04050052030889 - EBERLE | 2018-07-31 Meniscus Cutter 4,2 |
| 04050052030957 - EBERLE | 2018-07-31 Aggressive Meniscus Cutter 4,2 |
| 04050052030971 - EBERLE | 2018-07-31 Aggressive Meniscus Cutter 5,5 |
| 04050052031008 - EBERLE | 2018-07-31 Aggressive Meniscus Cutter Plus 4,2 |
| 04050052030865 - EBERLE | 2018-07-31 Round Burr 5,5 |
| 04050052030988 - EBERLE | 2018-07-31 Oval Burr 5,5 |