Medtronic Retrieval Snare Kit System
Catalogue number 00884450572122, listed by Merit Medical Systems, Inc., United States, under Device, Percutaneous Retrieval. 1 manufacturer in China is registered for this product code.
1manufacturer
1catalogue number
5510(k) clearances naming this product code
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 | Merit Medical Systems, 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, Complaint-file establishment, Manufacturer, Exporter |
| Record published | 2022-04-27 |
| Record revised | 2024-10-14 (version 2) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Supplied as a kit | Yes |
| Label carries | lot or batch number, expiry date |
| Packaging | Pack of 20 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 00884450572122 | Catheter French Size (F)-6F | 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 |
|---|---|
| K193507 | 2020-01-17 |
| K151497 | 2015-07-01 |
| K142265 | 2014-11-13 |
| K122088 | 2012-12-05 |
| K092343 | 2009-08-07 |
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.