| Primary Device ID | 70887868226150 |
| NIH Device Record Key | 5ac62447-b282-4b96-b844-6b2d750e2114 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MAXBRAID™ |
| Version Model Number | 900337 |
| Catalog Number | 900337 |
| Company DUNS | 129278169 |
| Company Name | Biomet Orthopedics, LLC |
| Device Count | 10 |
| 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 | 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00887868226151 [Primary] |
| GS1 | 70887868226150 [Unit of Use] |
| GAT | SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2021-02-05 |
| Device Publish Date | 2020-05-20 |
| 00889024703926 - Trocar K-Wire | 2025-12-25 |
| 00889024703933 - Trocar K-Wire | 2025-12-25 |
| 00889024703957 - Trocar K-Wire | 2025-12-25 |
| 00889024703223 - Modular Arthrodesis Nail | 2025-12-17 |
| 00889024703247 - Modular Arthrodesis Nail | 2025-12-17 |
| 00889024703278 - OSS™ Orthopedic Salvage System | 2025-12-17 |
| 00889024703308 - OSS™ Orthopedic Salvage System | 2025-12-17 |
| 00889024703728 - Versa-Dial® Shoulder System | 2025-12-17 |