# Becton Dickinson Canada Inc. (foreign exporter, Mississauga Ontario, CA): 12 new FDA device listings, incl. computer, diagnostic, programmable

**Score:** 55/100

| Field | Value |
|---|---|
| Establishment | Becton Dickinson Canada Inc. |
| Owner / operator | Becton Dickinson and Company |
| Role | Foreign exporter |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device |
| Location | Mississauga Ontario, CA |
| New listings | 12 |
| Devices | Computer, Diagnostic, Programmable; Stylet For Catheter, Gastro-Urology; System, Measurement, Blood-Pressure, Non-Invasive; Adjunctive Open Loop Fluid Therapy Recommender; Medium-Term Adjunctive Predictive Cardiovascular Indicator; Cerebral Oximeter; Adjunctive Predictive Cardiovascular Indicator; Oximeter, Tissue Saturation; Catheter, Oximeter, Fiber-Optic; Catheter, Flow Directed |
| Product codes | DQK, EZB, DXN, QMS, QNL, QEM, QAQ, MUD, DQE, DYG, DSB, FLL |
| Device classes | Class I, Class II |
| Medical specialties | Cardiovascular, Gastroenterology, Urology, General Hospital |
| Brand names | Hemosphere; SOLO PLUS Stiff Hybrid Guidewires; Hemosphere Alta |
| First new listing | 2026-09-11 |
| Latest new listing | 2026-09-11 |
| FDA registration number | 3045891669 |
| Registration expires | 2026-12-31 |

## Why this score
- 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: 2026-10-28T20:51:27.468Z.
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.