FDA device listing
ZITRIDERM- ANTIMICROBIAL HAND RUB,ZITRIDYL - ANTIMICROBIAL SPRAY,Zitrifect - Antimicrobial Inhaler,ZITRIFIQX…
FDA device listing 1897693095 · Gesco Healthcare Private Limited
Key facts
| Proprietary names | ZITRIDERM- ANTIMICROBIAL HAND RUB,ZITRIDYL - ANTIMICROBIAL SPRAY,Zitrifect - Antimicrobial Inhaler,ZITRIFIQX - ANTIMICROBIAL WASH,ZITRIFLO- Antimicrobial Disinfectant for floor and wall,Zitrifog - Antimicrobial Spray,Zitrifresh - Disinfectant for food items,Zitrigaurd - Antimicrobial Multi-surface Disinfectant Spray,Zitrimist - Antimicrobial Air Disinfectant Spray,Zitrinase - Antimicrobial Nasal… |
|---|---|
| Owner/operator | Gesco Healthcare Private Limited |
| Owner/operator number | 9032080 |
| Product codes | LRJ |
| Device names | LRJ - Disinfectant, Medical Devices |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.6890 |
| Review panels | General Hospital |
| Registered establishments | Gesco Healthcare Private Limited |
| Establishment registrations | 9613926 |
| FEI numbers | 1000402972 |
| Establishment operations | Contract Manufacturer, Foreign Exporter, 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