FDA device listing
Cruitiba Esterilizacao De Materiais Medicos
FDA device listing 1776432288 · Curitiba Esterilizacao De Materiais Medicos LTDA
Key facts
| Proprietary names | Cruitiba Esterilizacao De Materiais Medicos |
|---|---|
| Owner/operator | Curitiba Esterilizacao De Materiais Medicos LTDA |
| Owner/operator number | 10045352 |
| Product codes | NDP |
| Device names | NDP - Accessories, Implant, Dental, Endosseous |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.3980 |
| Review panels | Dental |
| Registered establishments | CURITIBA ESTERILIZACAO DE MATERIAIS MEDICOS LTDA |
| Establishment registrations | 3010596333 |
| FEI numbers | 3010596333 |
| 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