| Primary Device ID | 00880304341807 |
| NIH Device Record Key | 059424c7-e427-4bb0-8873-124395842da9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AGC MODULAR TIBIAL II |
| Version Model Number | 32-468419 |
| Catalog Number | 32-468419 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)348-9500 |
| customerservice@zimmerbiomet.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00880304341807 [Primary] |
| FZY | HAMMER, SURGICAL |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00880304341807]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-07-28 |
| 00880304341821 | 32-468421 |
| 00880304341807 | 32-468419 |
| 00880304341760 | 32-468414 |
| 00880304341746 | 32-468412 |
| 00880304341739 | 32-468411 |
| 00880304341661 | 32-468403 |
| 00880304341654 | 32-468401 |
| 00880304330283 | 32-349026 |
| 00880304330276 | 32-349025 |
| 00880304330269 | 32-349024 |
| 00880304330252 | 32-349023 |
| 00880304330245 | 32-349022 |
| 00880304004139 | 32-468402 |
| 00880304341722 | 32-468410 |
| 00880304343436 | 32-470190 |
| 00880304343375 | 32-470170 |
| 00880304342217 | 32-468522 |
| 00880304341647 | 32-468400 |
| 00880304341524 | 32-468387 |
| 00880304341777 | 32-468416 |
| 00880304341715 | 32-468409 |