SUTURE SNARE
- Primary DI
- 10845854035702
- Brand
- SUTURE SNARE
- Company
- Conmed Corporation
- Model
- GU1003
- Catalog number
- GU1003
- Device description
- SUTURE SNARE
- Published
- 2020-09-24
- 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 |
|---|---|
| GFA | BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| GFA | Blade, Saw, General & Plastic Surgery, Surgical | General, Plastic Surgery | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 20845854035709 | Direct Marking | GS1 | 0 | |
| 10845854035702 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized |
|---|---|
| 20845854035709 | 20845854035709 |
| 10845854035702 | 10845854035702 |
GMDN Terms#
| Term | Definition |
|---|---|
| Suturing unit, reusable | 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 reusable device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Length | 138 | Millimeter |
| Outer Diameter | 3.5 | Millimeter |
Storage And Handling#
| Type | Low | High | Condition |
|---|---|---|---|
| Special Storage Condition, Specify | 0 | 0 | KEEP DRY |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(800)237-0169 | CUSTOMER_SERVICE@CONMED.COM |
Regulatory Flags#
- DUNS number
- 071595540
- Device count
- 1
- Premarket exempt
- true
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
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|---|---|---|---|---|
| 30845854655478 | ConMed Airseal | SHELF-ICART | SHELF-ICART | 2026-09-18 |
| 20845854082482 | Paradigm | PEZS01A | PEZS01A | 2020-11-16 |
| 20845854015466 | SEQUENT | MR007C | MR007C | 2015-10-24 |
| 20845854036584 | SEQUENT | MR004C | MR004C | 2015-10-24 |
| 10653405044703 | CORE DYNAMICS | CD1406 | CD1406 | 2026-03-23 |
| 10653405045083 | CORE DYNAMICS | CD1608FH | CD1608FH | 2026-03-24 |
| 20653405990908 | GENESYS™ CrossFT™ | CFBC-4502R | CFBC-4502R | 2026-07-31 |
| 20653405990915 | GENESYS™ CrossFT™ | CFBC-4503R | CFBC-4503R | 2026-07-31 |
| 20653405990922 | GENESYS™ CrossFT™ | CFBC-5502R | CFBC-5502R | 2026-07-31 |
| 20653405990939 | GENESYS™ CrossFT™ | CFBC-5503R | CFBC-5503R | 2026-07-31 |
| 20653405990946 | GENESYS™ CrossFT™ | CFBC-6502R | CFBC-6502R | 2026-07-31 |
| 20653405990953 | GENESYS™ CrossFT™ | CFBC-6503R | CFBC-6503R | 2026-07-31 |
| 10653405000242 | YANKAUER | 0034470 | 0034470 | 2016-09-24 |
| 10845854035559 | E9000 | E9015 | E9015 | 2026-03-24 |
| 20653405008559 | CONMED | 60-0824-001 | 60-0824-001 | 2016-09-24 |
| 30653405003230 | CONMED | 138011 | 138011 | 2016-09-24 |
| 30653405003247 | CONMED | 138012 | 138012 | 2016-09-24 |
| 30653405058230 | AER DEFENSE | 60-8084-001 | 60-8084-001 | 2016-09-24 |
| 30845854655492 | PlumeSafe® X5™ | PX5-1354-22 | PX5-1354-22 | 2026-07-23 |
| 20845854042004 | Y-KNOT | YH01 | YH01 | 2015-10-24 |
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