Triple-Loop Snare Retrieval Kit
Triple-Loop Snare Retrieval Kit removes retrievable inferior vena cava filters that are no longer medically required through a percutaneous jugular approach. The expanded triple-loop snare…
Triple-Loop Snare Retrieval Kit removes retrievable inferior vena cava filters that are no longer medically required through a percutaneous jugular approach. The expanded triple-loop snare is 30 mm and is preloaded in a 7 Fr snare catheter.
The kit includes a 9 Fr inner sheath, 11 Fr outer sheath, 8 Fr dilator, hemostasis valve, high-pressure stopcock, Tuohy-Borst Y adapter and torque handle.
Fluoroscopic Features
The snare loops are radiopaque, and distal marker bands on the catheter and sheaths support fluoroscopic visualization. The kit is not made with natural rubber latex. The maximum recommended contrast power-injection rate is 15 mL per second.
Who Else Makes It
Registered in Guangdong.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Lifetech Scientific (Shenzhen) Co,.ltd | Shenzhen | Guangdong | Manufacturer | 3 |
Record
| Listed by | Argon Medical Devices, Inc., United States |
|---|---|
| FDA product code | MMX |
| Device type | Device, Percutaneous Retrieval |
| Device class | Class 2 |
| Regulation | 21 CFR 870.5150 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Manufacturer |
| 510(k) | K191758 |
| Record published | 2021-06-16 |
| Record revised | 2026-05-11 (version 3) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Label carries | lot or batch number, expiry date, manufacturing date |
| Storage | Special storage condition: Keep dry and away from sunlight |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 380911330 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| ONE Snare® | Merit Medical Systems, Inc. | 29 |
| EN Snare® | Merit Medical Systems, Inc. | 17 |
| SeQureTM Snare System | Lifetech Scientific (Shenzhen) Co,.ltd | 12 |
| Expro Elite | Teleflex Medical LLC | 10 |
| Halo™ Single Loop Snare Kit | Argon Medical Devices, Inc. | 9 |
| Atrieve™ Vascular Snare Kit | Argon Medical Devices, Inc. | 7 |
| Halo™ Single-Loop Microsnare Kit | Argon Medical Devices, Inc. | 6 |
| Expro Elite™ snare | Vascular Solutions LLC | 5 |
| Amplatz Goose Neck™ | Medtronic, Inc. | 5 |
| Sympro Elite | Teleflex Medical LLC | 5 |
| Quattro Elite™ snare | Vascular Solutions LLC | 5 |
| Sympro Elite™ snare | Vascular Solutions LLC | 5 |
Showing 12 of 26. All products under Device, Percutaneous Retrieval
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K232443 | 2023-09-07 |
| K200963 | 2021-01-05 |
| K200268 | 2020-06-03 |
| K191758 | 2019-12-17 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.