FDA device listing
MULTISAFE
FDA device listing 1218000110 · MULTISAFE SDN BHD
Key facts
| Proprietary names | MULTISAFE |
|---|---|
| Owner/operator | MULTISAFE SDN BHD |
| Owner/operator number | 9039578 |
| Premarket submissions | K001497 |
| Product codes | LZA |
| Device names | LZA - Polymer Patient Examination Glove |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.6250 |
| Review panels | General Hospital |
| Registered establishments | MULTISAFE SDN BHD |
| Establishment registrations | 9615095 |
| FEI numbers | 3004360380 |
| Establishment operations | Foreign Exporter, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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