FDA device listing
LABOMEX MBP
FDA device listing 1778250107 · AVANTTI MEDI CLEAR MBP, S.A.P.I. DE C.V.
Key facts
| Proprietary names | LABOMEX MBP |
|---|---|
| Owner/operator | AVANTTI MEDI CLEAR MBP, S.A.P.I. DE C.V. |
| Owner/operator number | 10053515 |
| Product codes | JRC |
| Device names | JRC - Micro Pipette |
| Device class | Class I |
| Classification regulations (21 CFR) | 862.2050 |
| Review panels | Clinical Chemistry |
| Registered establishments | AVANTTI MEDI CLEAR MBP, S.A.P.I. DE C.V. |
| Establishment registrations | 3013546453, 3043534762 |
| FEI numbers | 3013546453, 3043534762 |
| Establishment operations | Contract Sterilizer |
| 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