Establishment registration
CENTERPIECE S. DE R.L DE C.V (sterilization site)
FDA establishment registration 3019807891 · Tijuana Baja California, MX
Key facts
| Registration number | 3019807891 |
|---|---|
| Establishment name | CENTERPIECE S. DE R.L DE C.V (sterilization site) |
| Owner/operator | Centerpiece Holdings LLC |
| Owner/operator number | 10061801 |
| FEI number | 3019807891 |
| Address | Bulevar La Encantada Industrial, Parque Industrial El Florido, Seccion La Encantada #11530 |
| City | Tijuana Baja California |
| Country | MX |
| Registration valid through | 2026 |
| Product codes listed | CAC, DQO, DQY, DRA, DRE, DRF, DRY, DSQ, DTL, DTN, DTP, DTQ, DTR, DTZ, DWA, DWE, DWF, DWM, DXC, DXT, DYB, DZL, EOQ, EXF, EZW, FCG, FGB, FMF, FPA, FPK and 58 more |
| Device classes | 1, 2, 3, U |
At a glance
- 100–999 Device listings
- None UDI devices (GUDID)
- Current Registration current
- 1–9 FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database