FDA device listing
10 mL Oral Dose Syringe, KANGAROO, CARDINAL HEALTH, MONOJECT,17331/25,17335/50,17522/100,17522/50,17523/100,4oz 120cc…
FDA device listing 1272332289 · Sotera Health LLC
Key facts
| Proprietary names | 10 mL Oral Dose Syringe, KANGAROO, CARDINAL HEALTH, MONOJECT,17331/25,17335/50,17522/100,17522/50,17523/100,4oz 120cc Specimen/Medicine Cup w/ Screw Top Lid,Container, Liquid Medication, Graduated,D002896,MEDICINE CUP |
|---|---|
| Owner/operator | Sotera Health LLC |
| Owner/operator number | 10029425 |
| Product codes | KYW |
| Device names | KYW - Container, Liquid Medication, Graduated |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.6430 |
| Review panels | General Hospital |
| Registered establishments | Sterigenics U.S., LLC, Sterigenics US LLC, Sterigenics US, LLC |
| Establishment registrations | 1058584, 1061124, 1423662, 1526534, 2029275, 3004111573 |
| FEI numbers | 1526534, 1000219637, 1000306431, 1000512168, 3000215273, 3004111573 |
| Establishment operations | Contract Sterilizer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database