The NexSite™ HD, Hemodialysis Split Tip Catheter for long term use is a dual lumen, split tip radiopaque polyurethane catheter which contains a Dacron biomaterial cuff and two female luer…
The NexSite™ HD, Hemodialysis Split Tip Catheter for long term use is a dual lumen, split tip radiopaque polyurethane catheter which contains a Dacron biomaterial cuff and two female luer connectors. The DISC (Dermal Ingrowth Support Collar) assists with the direction of the catheter and consists of a biomaterial tissue ingrowth scaffold. The biomaterial scaffolds on the catheter shaft and DISC are aligned and facilitate tissue ingrowth, which is considered important in reducing the source of extraluminal infection in patients requiring long term catheterisation. The Catheter, DISC and the following ancillary components required for the procedure (0.038” guidewire, Stainless Steel Tunneler and Sleeve, 17Fr Introducer / Dilator and Luer Caps) are provided in a tray, sealed with a Tyvek lid and placed in a second sterile pouch so that the tray can be delivered to the sterile field
Who Else Makes It
All of them in Guangdong. One is registered as a contract manufacturer, able to build to a specification.
Record
Regulatory record for NexSite HD Split Tip Catheter | Listed by | Marvao Medical Devices Ltd., Ireland |
| FDA product code | MSD |
| Device type | Catheter, Hemodialysis, Implanted |
| Device class | Class 2 |
| Regulation | 21 CFR 876.5540 |
| Establishment | Specification developer, Complaint-file establishment, Manufacturer |
| Record published | 2015-04-20 |
| Record revised | 2021-02-05 (version 4) |
Specifications
Specifications | MRI safety | MR Safe |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Label carries | lot or batch number, expiry date |
| Packaging | Carton with 5 units of 5 |
| Sizes | Length 32 cm |
Recalls
1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
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.