| Primary Device ID | 04260397089316 |
| NIH Device Record Key | 2e675ecb-89ec-49b1-acc8-bf349fdb2909 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EIT ALIT Trial |
| Version Model Number | AET31534 |
| Company DUNS | 313088331 |
| Company Name | EIT Emerging Implant Technologies GmbH |
| 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 | 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04260397089316 [Primary] |
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04260397089316]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-02-07 |
| Device Publish Date | 2018-09-20 |
| 04260557770009 - EIT CIF cage | 2020-02-24 EIT CIF cage, H 5mm, 0°, S |
| 04260557770016 - EIT CIF cage | 2020-02-24 EIT CIF cage, H 5mm, 0°, S |
| 04260557770023 - EIT CIF cage | 2020-02-24 EIT CIF cage, H 6mm, 0°, S |
| 04260557770030 - EIT CIF cage | 2020-02-24 EIT CIF cage, H 7mm, 0°, S |
| 04260557770047 - EIT CIF cage | 2020-02-24 EIT CIF cage, H 8mm, 0°, S |
| 04260557770054 - EIT CIF cage | 2020-02-24 EIT CIF cage, H 9mm, 0°, S |
| 04260557770061 - EIT CIF cage | 2020-02-24 EIT CIF cage, H 10mm, 0°, S |
| 04260557770078 - EIT CIF cage | 2020-02-24 EIT CIF cage, H 11mm, 0°, S |