UDI device identifier
Rite Aid 8024512
UDI device identifier 00011822001670 · RITE AID CORPORATION
Key facts
| Primary DI | 00011822001670 |
|---|---|
| Brand name | Rite Aid |
| Version or model | 8024512 |
| Company | RITE AID CORPORATION |
| DUNS number | 014578892 |
| Product code | NFW |
| GMDN term | Amphetamine/methamphetamine group IVD, kit, rapid ICT, clinical |
| Device class | 2 | U |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jan 29, 2025 |
| Version date | Feb 6, 2025 |
| Description | Home Drug Test 14 Panel THC/COC/PCP/mAMP/AMP/MDMA/TCA/BAR/BZO/MTD/OXY/PPX/BUP/OPI |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 100–999 GUDID devices with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About UDI device identifiers (GUDID)
The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.
Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date: