FDA device listing
Occlutech®
FDA device listing 1311114593 · Medicoplast International GmbH
Key facts
| Proprietary names | Occlutech® |
|---|---|
| Owner/operator | Medicoplast International GmbH |
| Owner/operator number | 9035331 |
| Product codes | OZG |
| Device names | OZG - Transcatheter Septal Occluder (Atrial) |
| Device class | Class III |
| Classification regulations (21 CFR) | ORCA1.OZG |
| Review panels | Cardiovascular |
| Registered establishments | MEDICOPLAST INTERNATIONAL GMBH |
| Establishment registrations | 9617429 |
| FEI numbers | 3002807584 |
| 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