N/A
- Primary DI
- 00889095731934
- Brand
- N/A
- Company
- GLOBUS MEDICAL, INC.
- Model
- 604.105
- Device description
- Trial, SUSTAIN-R Oblique, 26mm Length, 5mm
- Published
- 2020-06-15
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
Product Codes#
| Code | Name |
|---|---|
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| LXH | Orthopedic Manual Surgical Instrument | Orthopedic | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00889095731934 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00889095731934 | 00889095731934 | 889095731934 | 0889095731934 |
GMDN Terms#
| Term | Definition |
|---|---|
| Surgical implant template, reusable | A device designed to determine the appropriate size and placement of a non-dental implant for a patient prior to or during implantation surgery. It is typically available as a graduated set or an individual plate (e.g., a translucent plastic sheet or a cut metal shape) with patterns/sizes corresponding to the size of the implant to be used to aid the surgeon in final selection of implant size, placement, and/or adaption. It is used for, e.g., total- or partial-joint prostheses, bone fracture fixation implants (plates, nails, including skull plate implants) or other types of surgical implants. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Regulatory Flags#
- DUNS number
- 139105691
- Device count
- 1
- Premarket exempt
- true
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00889095205831 | XEMPLIFI | 8103.0001S | 2015-10-10 | |
| 00889095205848 | XEMPLIFI | 8103.0005S | 2015-10-10 | |
| 00889095205855 | XEMPLIFI | 8103.0010S | 2015-10-10 | |
| 00889095205862 | XEMPLIFI | 8103.0101S | 2015-10-10 | |
| 00889095205879 | XEMPLIFI | 8103.0105S | 2015-10-10 | |
| 00889095205886 | XEMPLIFI | 8103.0110S | 2015-10-10 | |
| 00889095205893 | XEMPLIFI | 8103.0201S | 2015-10-10 | |
| 00889095205909 | XEMPLIFI | 8103.0203S | 2015-10-10 | |
| 00889095205916 | XEMPLIFI | 8103.0208S | 2015-10-10 | |
| 00889095205923 | XEMPLIFI | 8103.0210S | 2015-10-10 | |
| 00889095401820 | ANTHEM | 2171.6509 | 2171.6509 | 2026-09-25 |
| 00889095401844 | ANTHEM | 2171.6511 | 2171.6511 | 2026-09-25 |
| 00889095401868 | ANTHEM | 2171.6513 | 2171.6513 | 2026-09-25 |
| 00889095401882 | ANTHEM | 2171.6515 | 2171.6515 | 2026-09-25 |
| 00889095401905 | ANTHEM | 2171.6517 | 2171.6517 | 2026-09-25 |
| 00889095401929 | ANTHEM | 2171.6519 | 2171.6519 | 2026-09-25 |
| 00889095402285 | ANTHEM | 2171.6555 | 2171.6555 | 2026-09-25 |
| 00889095402438 | ANTHEM | 2171.6570 | 2171.6570 | 2026-09-25 |
| 00889095402483 | ANTHEM | 2171.6575 | 2171.6575 | 2026-09-25 |
| 00889095402537 | ANTHEM | 2171.6580 | 2171.6580 | 2026-09-25 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 00190776434762 | Millennium | Avalign Technologies, Inc. | LXH | 2026-10-12 |
| 00850080243176 | OSTEOROD Delivery System | BONE SOLUTIONS, INC. | LXH | 2026-10-12 |
| 00889795150264 | APEX 3D Total Ankle Replacement System | Paragon 28, Inc. | LXH | 2026-10-12 |
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| B0842003000020 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000030 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000100 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000110 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000120 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000130 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000200 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000210 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000220 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000230 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000300 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
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| B0842003000330 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000400 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000410 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000420 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000430 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000500 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000510 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000520 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000530 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000600 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000610 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |
| B0842003000620 | Keos Lumbar Instrument | KEOS | LXH | 2023-02-10 |