UDI device identifier
Harris Teeter 73429
UDI device identifier 00072036734297 · Harris Teeter, LLC
Key facts
| Primary DI | 00072036734297 |
|---|---|
| Brand name | Harris Teeter |
| Version or model | 73429 |
| Company | Harris Teeter, LLC |
| DUNS number | 048463103 |
| Product code | LCX |
| GMDN term | Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Feb 27, 2026 |
| Version date | Mar 30, 2026 |
| Description | Home Pregnancy Test |
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: