FDA device listing
Compact Arterial Catheterization Kit,EMS Chest Tube Insertion Kit, 24F,FORWARD® EMS Chest Tube Insertion Kit…
FDA device listing 1463789671 · Integrated Medcraft LLC
Key facts
| Proprietary names | Compact Arterial Catheterization Kit,EMS Chest Tube Insertion Kit, 24F,FORWARD® EMS Chest Tube Insertion Kit, 28Fr,FORWARD® Finger Thoracostomy Kit-Bilateral,FORWARD® Finger Thoracostomy Kit - Single Side |
|---|---|
| Owner/operator | Integrated Medcraft LLC |
| Owner/operator number | 10089406 |
| Product codes | PYI |
| Device names | PYI - Thoracic Catheter Insertion Tray |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4200 |
| Review panels | General & Plastic Surgery |
| Registered establishments | INTEGRATED MEDCRAFT LLC |
| Establishment registrations | 3030078769 |
| FEI numbers | 3030078769 |
| Establishment operations | Repackager/Relabeler |
| 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