PROFIX
- Primary DI
- 03596010224323
- Brand
- PROFIX
- Company
- Smith & Nephew, Inc.
- Model
- 71512574
- Catalog number
- 71512574
- Device description
- PROFIX 3/16IN HEX SCREWDRIVER
- Published
- 2015-08-30
- Public version status
- Update
- Distribution status
- 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 |
|---|---|---|---|---|
| 03596010224323 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 03596010224323 | 03596010224323 | 3596010224323 |
GMDN Terms#
| Term | Definition |
|---|---|
| Surgical screwdriver, reusable | A non-powered tool intended to fit into a screw head (e.g., slotted, cross/hex head) for the application of rotation to introduce/remove a screw (e.g., craniofacial bone screw, dental screw) into/from a patient in association with a surgical procedure [e.g., orthopaedic, dental, computer assisted surgery (CAS), image registration]. It may also be used to connect/disconnect a device to/from another device attached to a patient (e.g., implant component, fiducial marker). The proximal end of the device may have a handle for manual use or a profiled tang that fits into an independent chuck or power driver; it is typically made of metallic and/or polymer materials. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)821-5700 | 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 |
|---|---|---|---|---|
| 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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