PROFIX
- Primary DI
- 03596010534026
- Brand
- PROFIX
- Company
- Smith & Nephew, Inc.
- Model
- 71513368
- Catalog number
- 71513368
- Device description
- PROFIX MIS 5-IN-1 STANDARD EXTERNAL ROT GDE LEFT
- Published
- 2015-08-30
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| HRY | Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K121393 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 03596010534026 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 03596010534026 | 03596010534026 | 3596010534026 |
GMDN Terms#
| Term | Definition |
|---|---|
| Orthopaedic prosthesis implantation 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. It may be used for the following applications: 1) to hold/align/fix bone preparation instruments, prosthesis, or prosthesis component; 2) to provide relative position landmarks; 3) to ascertain correct spatial orientation or limb alignment; and/or 4) as an interface between prosthesis components. This is a reusable device intended to be sterilized prior to use. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)821-5700 | gudid@smith-nephew.com |
| +1(800)238-7538 | GUDID@SMITH-NEPHEW.COM |
Regulatory Flags#
- DUNS number
- 045483575
- Device count
- 1
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 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 |
| 00885556906293 | EVOS | 70879155 | 70879155 | 2026-06-25 |
| 00885556906309 | EVOS | 70879160 | 70879160 | 2026-06-25 |
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| 07613327127560 | INSTRUMENT | Howmedica Osteonics Corp. | HRY | 2017-11-24 |
| 07613327127607 | INSTRUMENT | Howmedica Osteonics Corp. | HRY | 2017-11-24 |
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