2 catalogue numbers from 85900PST, listed by Stryker Sustainability Solutions, United States, under Catheter, Ultrasound, Intravascular. 4 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Jiangsu (3), Shanghai (1). One is registered as a contract manufacturer, able to build to a specification.
Record
Regulatory record for Philips Healthcare | Listed by | Stryker Sustainability Solutions, United States |
| FDA product code | OBJ |
| Device type | Catheter, Ultrasound, Intravascular |
| Device class | Class 2 |
| Regulation | 21 CFR 870.1200 |
| Establishment | Reprocessor, Specification developer, Manufacturer |
| 510(k) | K223026 |
| Record published | 2025-02-11 |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | expiry date, serial number |
| Packaging | Case of 10 |
| UDI direct marking | Exempt |
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.