Catalogue number BRW084132-01, listed by Stryker GmbH, Switzerland, under Catheter, Percutaneous, Neurovasculature. 6 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Shanghai (4), Jiangsu (2). One is registered as a contract manufacturer, able to build to a specification.
Record
Regulatory record for Broadway 8 | Listed by | Stryker GmbH, Switzerland |
| FDA product code | QJP |
| Device type | Catheter, Percutaneous, Neurovasculature |
| Device class | Class 2 |
| Regulation | 21 CFR 870.1250 |
| Establishment | Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer |
| 510(k) | K241768 |
| Record published | 2025-01-24 |
| Record revised | 2026-05-05 (version 2) |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
| Storage | Special storage condition: Store in cool, dry, dark place. |
| Sizes | Length 132 cm; lumen/inner diameter 0.084 in |
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.