EXPert Nail
- Primary DI
- 10886982081353
- Brand
- EXPert Nail
- Company
- Synthes GmbH
- Model
- 04.003.003
- Catalog number
- 04003003
- Device description
- 12MM TI END CAP T40 STARDRIVE 15MM EXT FOR FEMORAL NAILS-EX
- Published
- 2015-09-14
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Contact Domains#
Product Codes#
Product Code Classifications#
Premarket Submissions#
Premarket Details#
| Submission | Supplement | Device | Applicant | Decision date | Product code |
|---|---|---|---|---|---|
| K033618 | 000 | SYNTHES (USA) RETROGRADE/ANTEGRADE FEMORAL NAIL SYSTEM | Synthes (Usa) | 2004-02-05 | HSB |
| K040336 | 000 | SYNTHES (USA) LATERAL ENTRY FEMORAL NAIL SYSTEM | Synthes (Usa) | 2004-04-12 | HSB |
| K172157 | 000 | DePuy Synthes Femoral Recon Nail System | Synthes (USA) Products, LLC | 2017-11-14 | HSB |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10886982081353 | Primary | GS1 | 0 | |
| H679040030030 | Secondary | HIBCC | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 10886982081353 | 10886982081353 |
GMDN Terms#
| Term | Definition |
|---|---|
| Bone nail implantable cap | A small, implantable, rounded plug, cover or threaded screw designed to seal the proximal end of an orthopaedic nail implanted to treat a damaged bone (e.g., a fracture), to prevent healing tissue from growing into the hollow nail and to facilitate nail extraction. Commonly known as an end-cap, it is typically made of metal [e.g., high-grade stainless steel, titanium (Ti)], and is available in a variety of sizes. It may also be used to securely lock the most proximal oblique locking screw or help extend the length of a nail when necessary. This is a single-use device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)255-2500 | xx@xx.xx |
Regulatory Flags#
- DUNS number
- 486711679
- Device count
- 1
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
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|---|---|---|---|---|
| 10887587078540 | NA | SD03.501.442 | SD03501442 | 2026-07-29 |
| 10886982362179 | NA | SD03.043.006 | SD03043006 | 2026-07-24 |
| 10887587078557 | NA | SD03.503.067 | SD03503067 | 2026-07-24 |
| 10887587078564 | NA | SD03.503.072 | SD03503072 | 2026-07-24 |
| 10705034712307 | NA | 03.604.002 | 03604002 | 2016-12-31 |
| 10705034712802 | NA | 03.606.011 | 03606011 | 2016-12-31 |
| 10705034714592 | NA | 03.613.012 | 03613012 | 2016-12-31 |
| 10705034767819 | VentroFix | 304.834 | 304834 | 2016-12-31 |
| 10705034768939 | NA | 314.064 | 314064 | 2016-12-31 |
| 10705034768960 | Click'X | 314.067 | 314067 | 2016-12-31 |
| 10705034768977 | Click'X | 314.068 | 314068 | 2016-12-31 |
| 10705034768984 | Click'X | 314.069 | 314069 | 2016-12-31 |
| 10705034769646 | NA | 328.026 | 328026 | 2016-12-31 |
| 10705034772608 | NA | 388.364 | 388364 | 2016-12-31 |
| 10705034775401 | NA | 389.288 | 389288 | 2016-12-31 |
| 10705034777375 | NA | 394.585 | 394585 | 2016-12-31 |
| 20705034764051 | NA | 292.020 | 292020 | 2019-08-29 |
| 00863176000317 | FIBULINK | FGS-1100 | FGS1100 | 2020-03-26 |
| 00863176000324 | FIBULINK | FGS-1300 | FGS1300 | 2020-03-26 |
| 00863176000300 | FIBULINK | FGS-1000 | FGS1000 | 2017-06-08 |
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