Universal Mandible AXS
- Primary DI
- 07613327567656
- Brand
- Universal Mandible AXS
- Company
- Stryker Leibinger GmbH & Co. KG
- Model
- 56-23514
- Catalog number
- 56-23514
- Device description
- Locking screws, AXS, self-tapping
- Published
- 2023-09-15
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- true
Product Codes#
| Code | Name |
|---|---|
| DZL | SCREW, FIXATION, INTRAOSSEOUS |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| DZL | Screw, Fixation, Intraosseous | Dental | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 37613327567657 | Primary | GS1 | 0 | |
| 07613327567656 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 37613327567657 | 37613327567657 | |
| 07613327567656 | 07613327567656 | 7613327567656 |
GMDN Terms#
| Term | Definition |
|---|---|
| Craniofacial bone screw, non-bioabsorbable | A small, threaded rod with a slotted head intended to be implanted in craniofacial bone (including the maxilla and/or mandible) for fracture fixation by direct interfragmentary stabilization of bone or by screwing plates in place; it may also be intended for transplanted bone fixation. It may be self-drilling/self-tapping and is made of a material that is not chemically degraded or absorbed via natural body processes [e.g., implant grade metal such as titanium (Ti)]. Its uses include repair of orbital fractures and fractures around the cranial sinuses, paediatric reconstructive surgery, craniotomy flap fixation, bone augmentation procedures. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 | |
| Length | 14 | Millimeter |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Regulatory Flags#
- DUNS number
- 316153956
- Device count
- 5
- DM exempt
- false
- 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 |
|---|---|---|---|---|
| 07613327465532 | NA | 92-00232 | 92-00232 | 2019-05-03 |
| 07613327465549 | NA | 92-00230 | 92-00230 | 2019-05-03 |
| 04546540134790 | NA | 01-03230 | 01-03230 | 2017-01-11 |
| 04546540134974 | NA | 01-04010 | 01-04010 | 2016-12-08 |
| 04546540134998 | NA | 01-04070 | 01-04070 | 2016-12-08 |
| 04546540135018 | NA | 01-04100 | 01-04100 | 2016-12-08 |
| 04546540138477 | NA | 01-09561 | 01-09561 | 2016-12-08 |
| 04546540141514 | NA | 01-15315 | 01-15315 | 2017-01-11 |
| 04546540143242 | NA | 01-19715 | 01-19715 | 2016-12-08 |
| 04546540143273 | NA | 01-19730 | 01-19730 | 2016-12-08 |
| 04546540166623 | NA | 09-01461 | 09-01461 | 2017-01-11 |
| 04546540166630 | NA | 09-01462 | 09-01462 | 2017-01-11 |
| 04546540215161 | NA | 37-10272 | 37-10272 | 2016-12-08 |
| 04546540215222 | NA | 37-10411 | 37-10411 | 2016-12-08 |
| 04546540215291 | NA | 37-10930 | 37-10930 | 2016-12-08 |
| 04546540215413 | NA | 37-12461 | 37-12461 | 2016-12-08 |
| 04546540217059 | NA | 41-36792 | 41-36792 | 2016-12-08 |
| 04546540217066 | NA | 41-36793 | 41-36793 | 2016-12-08 |
| 04546540217073 | NA | 41-36794 | 41-36794 | 2016-12-08 |
| 04546540217080 | NA | 41-36795 | 41-36795 | 2016-12-08 |
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