FDA device listing
Duotip-Test II Skin Test Applicator, Box of 400,Wells for Duotip-Test II Dipwell Tray, Pouch of 40
FDA device listing 1446946257 · MIDWEST STERILIZATION CORP.
Key facts
| Proprietary names | Duotip-Test II Skin Test Applicator, Box of 400,Wells for Duotip-Test II Dipwell Tray, Pouch of 40 |
|---|---|
| Owner/operator | MIDWEST STERILIZATION CORP. |
| Owner/operator number | 1928237 |
| Product codes | SCL |
| Device names | SCL - Allergen And Vaccine Delivery Needles |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.5570 |
| Review panels | General Hospital |
| Registered establishments | MIDWEST STERILIZATION CORP. |
| Establishment registrations | 1928237 |
| FEI numbers | 1928237 |
| 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