TWINFIX
- Primary DI
- 03596010448446
- Brand
- TWINFIX
- Company
- Smith & Nephew, Inc.
- Model
- 7209109
- Catalog number
- 7209109
- Device description
- 6.5 MM TITANIUM SINGLE ANCHOR, STERILE
- Published
- 2015-08-30
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| MBI | FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| MBI | Fastener, Fixation, Nondegradable, Soft Tissue | Orthopedic | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 03596010448446 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 03596010448446 | 03596010448446 | 3596010448446 |
GMDN Terms#
| Term | Definition |
|---|---|
| Suturing unit, single-use | A non-powered, hand-held device intended to pass sutures or a needle/suture assembly through tissues/prosthetic materials to facilitate suturing during an endoscopic and/or open surgical procedure; it may also knot, cut and/or tighten the sutures/ligature loop during or after placement. It typically consists of a shaft with hooks, catches, clasps, or forceps-like jaws at the distal end, and a proximal handle with controls. It typically has a pointed/cutting component to create a suture tunnel, and is loaded with the sutures or the suture is inserted through the shaft. This is a single-use device. |
Contacts#
| Phone | |
|---|---|
| +1(800)238-7538 | GUDID@SMITH-NEPHEW.COM |
Regulatory Flags#
- DUNS number
- 045483575
- Device count
- 1
- 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
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00885556919781 | Real Intelligence | ROB30007 | ROB30007 | 2026-10-13 |
| 00885556924327 | Real Intelligence | ROB30801 | ROB30801 | 2026-10-08 |
| 03596010445803 | NA | 7209030 | 7209030 | 2015-08-30 |
| 03596010470294 | SAPHYRE | 7209684 | 7209684 | 2015-08-30 |
| 03596010470331 | ABLATOR | 7209659 | 7209659 | 2015-08-30 |
| 03596010470348 | ABLATOR | 7209658 | 7209658 | 2015-08-30 |
| 03596010470416 | ABLATOR | 7209651 | 7209651 | 2015-08-30 |
| 03596010470577 | ABLATOR | 7209650 | 7209650 | 2015-08-30 |
| 03596010470614 | TAC-S | 7209632 | 7209632 | 2015-08-30 |
| 03596010470393 | ABLATOR | 7209653 | 7209653 | 2015-08-30 |
| 03596010470423 | ABLATOR | 7209649 | 7209649 | 2015-08-30 |
| 03596010510976 | NA | 7210040 | 7210040 | 2015-08-30 |
| 00885556236949 | STRUCSURE | 717805 | 717805 | 2016-04-08 |
| 00885556236994 | STRUCSURE | 717808 | 717808 | 2016-04-08 |
| 00885556237045 | STRUCSURE | 717816 | 717816 | 2016-04-08 |
| 00885556838211 | Total Foot System 2 | 2805007 | 2805007 | 2023-04-18 |
| 03596010619952 | NA | 72201597 | 72201597 | 2015-08-29 |
| 03596010619969 | NA | 72201598 | 72201598 | 2015-08-29 |
| 00885556572351 | NA | 72201597S | 72201597S | 2017-06-15 |
| 00885556572368 | NA | 72201598S | 72201598S | 2017-06-15 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 00888867627840 | Arthrex® | ARTHREX, INC. | MBI | 2026-10-07 |
| 00888867627857 | Arthrex® | ARTHREX, INC. | MBI | 2026-10-07 |
| 00888867627864 | Arthrex® | ARTHREX, INC. | MBI | 2026-10-07 |
| 00817337000586 | Integrity Retractable Implant Inserter | Anika Therapeutics, Inc. | MBI | 2026-10-05 |
| 20845854655501 | Argo Knotless | Conmed Corporation | MBI | 2026-09-25 |
| 20845854655518 | Argo Knotless | Conmed Corporation | MBI | 2026-09-25 |
| 00889024711280 | Jgrknt Reusable Fishmouth Perc Guide | Biomet Orthopedics, LLC | MBI | 2026-08-25 |
| 00889024712034 | Percutaneous Soft Anchor Short 1.4mm Guide | Biomet Orthopedics, LLC | MBI | 2026-08-25 |
| 00810198920178 | TeKBrace | TheraMicro, LLC | MBI | 2026-08-14 |
| 00811714036472 | Thunderbolt | RESPONSIVE ORTHOPEDICS LLC | MBI | 2026-07-31 |
| 00811714036489 | Thunderbolt | RESPONSIVE ORTHOPEDICS LLC | MBI | 2026-07-31 |
| 00810146164340 | Redifix | TRAX SURGICAL INC. | MBI | 2026-07-20 |
| 00810146164357 | Redifix | TRAX SURGICAL INC. | MBI | 2026-07-20 |
| 00810146164388 | Redifix | TRAX SURGICAL INC. | MBI | 2026-07-20 |
| 00810146164418 | Redifix | TRAX SURGICAL INC. | MBI | 2026-07-20 |
| 00810146164449 | Redifix | TRAX SURGICAL INC. | MBI | 2026-07-20 |
| 00810146164456 | Redifix | TRAX SURGICAL INC. | MBI | 2026-07-20 |
| 00810146164463 | Redifix | TRAX SURGICAL INC. | MBI | 2026-07-20 |
| 00810146164500 | Redifix | TRAX SURGICAL INC. | MBI | 2026-07-20 |
| 00810146164517 | Redifix | TRAX SURGICAL INC. | MBI | 2026-07-20 |
| 00810146164531 | Redifix | TRAX SURGICAL INC. | MBI | 2026-07-20 |
| 00810146164562 | Redifix | TRAX SURGICAL INC. | MBI | 2026-07-20 |
| 00810146164579 | Redifix | TRAX SURGICAL INC. | MBI | 2026-07-20 |
| 00810146164623 | Redifix | TRAX SURGICAL INC. | MBI | 2026-07-20 |
| 00810146164654 | Redifix | TRAX SURGICAL INC. | MBI | 2026-07-20 |
| 00810146164685 | Redifix | TRAX SURGICAL INC. | MBI | 2026-07-20 |
| 00810146164692 | Redifix | TRAX SURGICAL INC. | MBI | 2026-07-20 |
| 00860016070004 | ICONN Revolution 6.5MM Knotless Suture Anchor | ICONN ORTHOPEDICS LLC | MBI | 2026-07-16 |
| 10810128462867 | VersiTILT 2.4 x 8.5mm Implant System | T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION | MBI | 2026-07-16 |
| 10810128462874 | VersiTILT 2.4 x 8.5mm Button and Inserter | T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION | MBI | 2026-07-16 |