| Primary Device ID | 00193982567767 |
| NIH Device Record Key | 3697ce31-8d6a-4065-b4f5-ee4ab7b14111 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EXCELSIUSFLEX |
| Version Model Number | 6221.2503 |
| Company DUNS | 139105691 |
| Company Name | GLOBUS MEDICAL, INC. |
| 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 | 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 | 00193982567767 [Primary] |
| OLO | Orthopedic stereotaxic instrument |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00193982567767]
Moist Heat or Steam Sterilization
[00193982567767]
Moist Heat or Steam Sterilization
[00193982567767]
Moist Heat or Steam Sterilization
[00193982567767]
Moist Heat or Steam Sterilization
[00193982567767]
Moist Heat or Steam Sterilization
[00193982567767]
Moist Heat or Steam Sterilization
[00193982567767]
Moist Heat or Steam Sterilization
[00193982567767]
Moist Heat or Steam Sterilization
[00193982567767]
Moist Heat or Steam Sterilization
[00193982567767]
Moist Heat or Steam Sterilization
[00193982567767]
Moist Heat or Steam Sterilization
[00193982567767]
Moist Heat or Steam Sterilization
[00193982567767]
Moist Heat or Steam Sterilization
[00193982567767]
Moist Heat or Steam Sterilization
[00193982567767]
Moist Heat or Steam Sterilization
[00193982567767]
Moist Heat or Steam Sterilization
[00193982567767]
Moist Heat or Steam Sterilization
[00193982567767]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-12-25 |
| Device Publish Date | 2024-12-17 |
| 00193982567910 | Articulated Driver Tip |
| 00193982567903 | CT Registration Attachment, EFlex |
| 00193982567897 | Plane Checker Attachment, EFlex |
| 00193982567880 | Sawblade Calibration Attachment, EFlex |
| 00193982567873 | Tibia Hook Attachment, EFlex |
| 00193982567866 | Implant Verification Attachment, EFlex |
| 00193982567859 | Registration Stylus, EFlex |
| 00193982567842 | Quick-Connect Array, EFlex |
| 00193982567835 | Tibia Reference Array, EFlex |
| 00193982567828 | Femur Reference Array, EFlex |
| 00193982567811 | Robot Reference Array, EFlex |
| 00193982567774 | Sawblade Adapter, EFlex |
| 00193982567767 | End Effector Base Lock, EFlex |
| 00193982565428 | ExcelsiusFlex, 120V |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() EXCELSIUSFLEX 90903528 not registered Live/Pending |
Globus Medical, Inc. 2021-08-26 |