VORTEX
- Primary DI
- 03596010457073
- Brand
- VORTEX
- Company
- Smith & Nephew, Inc.
- Model
- 71270080
- Catalog number
- 71270080
- Device description
- VORTEX AND MIXOR NOZZLE STANDARD BREAKWAY
- Published
- 2015-08-29
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| KIH | DISPENSER, CEMENT |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KIH | Dispenser, Cement | Orthopedic | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 23596010457077 | Package | GS1 | 5 | In Commercial Distribution |
| 03596010457073 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 23596010457077 | 23596010457077 | |
| 03596010457073 | 03596010457073 | 3596010457073 |
GMDN Terms#
| Term | Definition |
|---|---|
| Orthopaedic prosthesis implantation positioning instrument, reusable | A hand-held surgical instrument intended to be used during implantation of an orthopaedic prosthesis, either manually or as a computer-assisted surgery (CAS) device, to aid in the navigation/placement of the prosthesis or other instruments [e.g., drill sleeves and guide wires (Kirschner wires), patella saw guide]. It may be used for the following applications: 1) to hold/align/fix/guide other instruments, prostheses, or prosthesis components; 2) to provide relative position landmarks; 3) to ascertain correct spatial orientation or limb alignment; and/or 4) as an interface (non-adaptive) between prosthesis components. This is a reusable device intended to be sterilized prior to use. |
Contacts#
| Phone | |
|---|---|
| +1(800)238-7538 | GUDID@SMITH-NEPHEW.COM |
Regulatory Flags#
- DUNS number
- 045483575
- Device count
- 1
- Premarket exempt
- true
- Lot or batch
- true
- Expiration date on label
- true
Other Devices From This Company#
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|---|---|---|---|---|
| 00885556165560 | NA | 76515310 | 76515310 | 2026-07-16 |
| 00885556923023 | NA | 76547001 | 76547001 | 2026-07-16 |
| 00885556925089 | NA | 74034445 | 74034445 | 2026-07-14 |
| 00885556925379 | CORIOGRAPH | ROB20032 | ROB20032 | 2026-07-08 |
| 00885556925386 | CORIOGRAPH | ROB20031 | ROB20031 | 2026-07-08 |
| 00885556904879 | EVOS | 70887105 | 70887105 | 2026-06-25 |
| 00885556904923 | EVOS | 70897130 | 70897130 | 2026-06-25 |
| 00885556906163 | EVOS | 70879090 | 70879090 | 2026-06-25 |
| 00885556906170 | EVOS | 70879095 | 70879095 | 2026-06-25 |
| 00885556906187 | EVOS | 70879100 | 70879100 | 2026-06-25 |
| 00885556906194 | EVOS | 70879105 | 70879105 | 2026-06-25 |
| 00885556906200 | EVOS | 70879110 | 70879110 | 2026-06-25 |
| 00885556906217 | EVOS | 70879115 | 70879115 | 2026-06-25 |
| 00885556906224 | EVOS | 70879120 | 70879120 | 2026-06-25 |
| 00885556906231 | EVOS | 70879125 | 70879125 | 2026-06-25 |
| 00885556906248 | EVOS | 70879130 | 70879130 | 2026-06-25 |
| 00885556906255 | EVOS | 70879135 | 70879135 | 2026-06-25 |
| 00885556906262 | EVOS | 70879140 | 70879140 | 2026-06-25 |
| 00885556906279 | EVOS | 70879145 | 70879145 | 2026-06-25 |
| 00885556906286 | EVOS | 70879150 | 70879150 | 2026-06-25 |
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| 08031497003801 | Mendec® Kypho Set Bilateral 10 mm | TECRES SPA | KIH | 2025-12-17 |
| 08031497003818 | Mendec® Kypho Set Bilateral 15 mm | TECRES SPA | KIH | 2025-12-17 |
| 08031497003825 | Mendec® Kypho Set Bilateral 20 mm | TECRES SPA | KIH | 2025-12-17 |
| 06923558507569 | Kyphoplasty Tool Kit | Jiangsu Changmei Medtech Co., Ltd. | KIH | 2025-10-23 |
| 06923558509693 | Kyphoplasty Tool Kit | Jiangsu Changmei Medtech Co., Ltd. | KIH | 2025-10-23 |
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