Lucent
- Primary DI
- 08406061018039
- Brand
- Lucent
- Company
- SPINAL ELEMENTS, INC.
- Model
- 11341-102
- Device description
- Lucent XP 10mm Shaft – Offset Inserter
- Published
- 2019-03-12
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Product Codes#
| Code | Name |
|---|---|
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | Orthopedic | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 08406061018039 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 08406061018039 | 08406061018039 | 8406061018039 |
GMDN Terms#
| Term | Definition |
|---|---|
| Orthopaedic implant inserter/extractor | A hand-held manual surgical instrument designed to insert or extract an implantable orthopaedic device (e.g., a bone nail, spiral blade, or bone fixation plate) through application of a striking or screwing force. It is an instrument in a one-piece or modular configuration with a mechanism that will attach and/or lock to part of the implant, and a mechanism to apply the striking force (e.g., on a pad/flange) using a surgical hammer or a weight that can slide along a shaft, or a mechanism for twisting (screwing) (e.g., T-handle). This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Regulatory Flags#
- DUNS number
- 610712213
- Device count
- 1
- DM exempt
- true
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- true
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00840606158213 | KARMA | 75310-000 | 2020-03-03 | |
| 00840466901196 | Primus | 66012-095-030 | 2026-03-27 | |
| 00840466901202 | Primus | 66012-095-035 | 2026-03-27 | |
| 00840466901219 | Primus | 66012-105-030 | 2026-03-27 | |
| 00840466901226 | Primus | 66012-105-035 | 2026-03-27 | |
| 00840466901233 | Primus | 66012-105-040 | 2026-03-27 | |
| 00840466901240 | Primus | 66012-105-045 | 2026-03-27 | |
| 00840466901257 | Primus | 66012-105-050 | 2026-03-27 | |
| 00840466901264 | Primus | 66012-105-055 | 2026-03-27 | |
| 00840466901271 | Primus | 66023-045-030 | 2026-03-27 | |
| 00840466901288 | Primus | 66023-045-035 | 2026-03-27 | |
| 00840466901295 | Primus | 66023-045-040 | 2026-03-27 | |
| 00840466901301 | Primus | 66023-045-045 | 2026-03-27 | |
| 00840466901318 | Primus | 66023-045-050 | 2026-03-27 | |
| 00840466901325 | Primus | 66023-055-025 | 2026-03-27 | |
| 00840466901332 | Primus | 66023-055-030 | 2026-03-27 | |
| 00840466901349 | Primus | 66023-055-035 | 2026-03-27 | |
| 00840466901356 | Primus | 66023-055-040 | 2026-03-27 | |
| 00840466901363 | Primus | 66023-055-045 | 2026-03-27 | |
| 00840466901370 | Primus | 66023-055-050 | 2026-03-27 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 00197157075989 | ZAVATION DISTRACTOR | Zavation LLC | MAX | 2026-05-28 |
| 00197157075996 | ZAVATION DISTRACTOR | Zavation LLC | MAX | 2026-05-28 |
| 00197157076009 | ZAVATION DISTRACTOR | Zavation LLC | MAX | 2026-05-28 |
| 00197157076016 | ZAVATION DISTRACTOR | Zavation LLC | MAX | 2026-05-28 |
| 00197157076023 | ZAVATION DISTRACTOR | Zavation LLC | MAX | 2026-05-28 |
| 00197157076030 | ZAVATION DISTRACTOR | Zavation LLC | MAX | 2026-05-28 |
| 00197157076047 | ZAVATION DISTRACTOR | Zavation LLC | MAX | 2026-05-28 |
| 00197157076054 | ZAVATION DISTRACTOR | Zavation LLC | MAX | 2026-05-28 |
| 00197157076061 | ZAVATION DISTRACTOR | Zavation LLC | MAX | 2026-05-28 |
| 00197157075859 | ZAVATION INSERTER | Zavation LLC | MAX | 2026-05-27 |
| 00810166522366 | X-PAC | EXPANDING INNOVATIONS, INC. | MAX | 2026-05-27 |
| 00810166522373 | X-PAC | EXPANDING INNOVATIONS, INC. | MAX | 2026-05-27 |
| B70712535005S0 | Dual X Graft Tamp Short | AMPLIFY SURGICAL, INC. | MAX | 2026-05-27 |
| B707129410010130 | DUALXS T/PLIF 15 DEG x 9-12MM | AMPLIFY SURGICAL, INC. | MAX | 2026-05-27 |
| B707129410010200 | DUALXS T/PLIF 18 DEG x 10-13MM | AMPLIFY SURGICAL, INC. | MAX | 2026-05-27 |
| 07613153046196 | AVS PL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046202 | AVS PL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046219 | AVS PL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046233 | AVS PL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046301 | AVS PL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046325 | AVS PL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046332 | AVS PL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046356 | AVS PL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046363 | AVS PL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046394 | AVS TL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046400 | AVS TL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046417 | AVS TL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046424 | AVS TL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046431 | AVS TL | Stryker Corporation | MAX | 2015-09-14 |
| 07613153046448 | AVS TL | Stryker Corporation | MAX | 2015-09-14 |