FDA device listing
LIFE TECHNOLOGIES CORPORATION
FDA device listing 1202880630 · Polimeros Formula de Tecate, SA de CV
Key facts
| Proprietary names | LIFE TECHNOLOGIES CORPORATION |
|---|---|
| Owner/operator | Polimeros Formula de Tecate, SA de CV |
| Owner/operator number | 10054378 |
| Product codes | KDT |
| Device names | KDT - Container, Specimen Mailer And Storage, Sterile |
| Device class | Class I |
| Classification regulations (21 CFR) | 864.3250 |
| Review panels | Pathology |
| Registered establishments | Polimeros Formula de Tecate S.A de C.V |
| Establishment registrations | 1000484830 |
| FEI numbers | 1000484830 |
| Establishment operations | Contract Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database