# Suzhou Prosteri Medical Technology Co., Ltd. (contract sterilizer, Suzhou Jiangsu, CN): 7 new FDA device listings, incl. device, vascular, for promoting embolization

**Score:** 70/100

| Field | Value |
|---|---|
| Establishment | Suzhou Prosteri Medical Technology Co., Ltd. |
| Owner / operator | Suzhou ProSteri Medical Technology Co., Ltd. |
| Role | Contract sterilizer |
| Establishment types | Sterilize Medical Device for Another Party (Contract Sterilizer) |
| Location | Suzhou Jiangsu, CN |
| New listings | 7 |
| Devices | Device, Vascular, For Promoting Embolization; Device, Neurovascular Embolization; Bronchoscope (Flexible Or Rigid); Catheters, Transluminal Coronary Angioplasty, Percutaneous; Cystoscope And Accessories, Flexible/Rigid; Ureteroscope And Accessories, Flexible/Rigid |
| Product codes | KRD, HCG, EOQ, LOX, FAJ, FGB |
| Device classes | Class II |
| Medical specialties | Cardiovascular, Neurology, Ear, Nose, Throat, Gastroenterology, Urology |
| Brand names | Numen™ Helia Coil Embolization System; NumenFR™ Detachment System; Broncho Videoscope System; Firefighter Pro PTCA Balloon Catheter; Urology Videoscope System; Single-use Flexible Ureteroscope SUV-5C-B |
| First new listing | 2026-06-08 |
| Latest new listing | 2026-09-02 |
| FDA registration number | 3017961114 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-11-04T21:52:36.524Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.