Product code
QIZ: Material, implantable for controlled release, cder or cber led
FDA product code · Not Classified · General Hospital
Key facts
| Product code | QIZ |
|---|---|
| Device | Material, implantable for controlled release, cder or cber led |
| Device class | Not Classified |
| Review panel | General Hospital |
| Submission type | Contact ODE |
| GMP exempt | No |
| Implanted device | No |
| Life-sustaining or life-supporting | No |
| Definition | Implantable material for controlled release of drug substance. |
At a glance
- None 510(k) clearances
- None De Novo grants
- None PMA approvals
- None HDE approvals
- 1–9 UDI devices (GUDID)
- None MAUDE adverse event reports
- None Recalled products (Z-numbers)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device product codes
FDA product codes classify medical devices by type and intended use; each code maps to a device class, a classification regulation and a review panel.
Source: U.S. Food and Drug Administration (FDA), Product Classification database