Establishment registration
MARTECH MEDICAL PRODUCTS S. DE RL. DE CV.
FDA establishment registration 3003915875 · MEXICALI Baja California, MX
Key facts
| Registration number | 3003915875 |
|---|---|
| Establishment name | MARTECH MEDICAL PRODUCTS S. DE RL. DE CV. |
| Owner/operator | MARTECH MEDICAL PRODUCTS |
| Owner/operator number | 2527072 |
| FEI number | 3003915875 |
| Address | CALLE MERCURIO N 46 |
| City | MEXICALI Baja California |
| Country | MX |
| Registration valid through | 2026 |
| Product codes listed | BSO, BSY, BZT, DOX, DQO, DQX, DQY, DRE, DWS, DXT, DYB, ENW, EYB, FAD, FAJ, FGB, FGY, FJS, FMI, FOZ, FPA, GAR, GBS, GBW, GBX, GBZ, GCJ, GDF, GES, GWG and 25 more |
| Device classes | 1, 2, 3, U |
At a glance
- 100–999 Device listings
- 10–99 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