| Primary Device ID | 00681490039017 |
| NIH Device Record Key | dd294672-95dc-4131-b66c-eade46e2fb38 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Bio-Flek |
| Version Model Number | 1358225 |
| Company DUNS | 835465063 |
| Company Name | MEDTRONIC XOMED, INC. |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00681490039017 [Primary] |
| EPW | Support, head, surgical, ENT |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-07-12 |
| Device Publish Date | 2021-07-04 |
| 00763000299118 | HEAD SUPPORT 1358227 BIOFLEK RISER |
| 00763000299101 | HEAD SUPPORT 1358225 BIOFLEK SURGICAL |
| 00681490039024 | HEAD SUPPORT 1358227 BIOFLEK RISER |
| 00681490039017 | HEAD SUPPORT 1358225 BIOFLEK SURGICAL |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() BIO-FLEK 73626253 1467164 Live/Registered |
TREACE MEDICAL, INC. 1986-10-21 |