NA
- Primary DI
- 23596010036111
- Brand
- NA
- Company
- Smith & Nephew, Inc.
- Model
- 110675
- Catalog number
- 110675
- Device description
- SWANSON SUTURE PASSER
- Published
- 2015-08-29
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| JDS | NAIL, FIXATION, BONE |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| JDS | Nail, Fixation, Bone | Orthopedic | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K983942 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 23596010036111 | Package | GS1 | 6 | In Commercial Distribution |
| 03596010036117 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 23596010036111 | 23596010036111 | |
| 03596010036117 | 03596010036117 | 3596010036117 |
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 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; it may in addition knot and/or cut the sutures as they are placed. This is a single-use device. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)238-7538 | GUDID@SMITH-NEPHEW.COM |
Regulatory Flags#
- DUNS number
- 109903521
- 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 |
|---|---|---|---|---|
| 03596010479235 | ECHELON | 71342011 | 71342011 | 2015-09-28 |
| 03596010479266 | ECHELON | 71342014 | 71342014 | 2015-09-28 |
| 03596010479273 | ECHELON | 71342015 | 71342015 | 2015-09-28 |
| 03596010479297 | ECHELON | 71342017 | 71342017 | 2015-09-28 |
| 03596010479303 | ECHELON | 71342018 | 71342018 | 2015-09-28 |
| 03596010479310 | ECHELON | 71342019 | 71342019 | 2015-09-28 |
| 03596010479341 | ECHELON | 71343012 | 71343012 | 2015-09-28 |
| 03596010459749 | SYNERGY | 71309109 | 71309109 | 2015-08-30 |
| 03596010459756 | SYNERGY | 71309110 | 71309110 | 2015-08-30 |
| 03596010459787 | SYNERGY | 71309113 | 71309113 | 2015-08-30 |
| 03596010459794 | SYNERGY | 71309114 | 71309114 | 2015-08-30 |
| 03596010459817 | SYNERGY | 71309116 | 71309116 | 2015-08-30 |
| 03596010459831 | SYNERGY | 71309118 | 71309118 | 2015-08-30 |
| 03596010479259 | ECHELON | 71342013 | 71342013 | 2015-09-28 |
| 03596010479280 | ECHELON | 71342016 | 71342016 | 2015-09-28 |
| 03596010479358 | ECHELON | 71343013 | 71343013 | 2015-09-28 |
| 03596010479365 | ECHELON | 71343014 | 71343014 | 2015-09-28 |
| 03596010479389 | ECHELON | 71343016 | 71343016 | 2015-09-28 |
| 03596010479396 | ECHELON | 71343017 | 71343017 | 2015-09-28 |
| 03596010479402 | ECHELON | 71343018 | 71343018 | 2015-09-28 |
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