FDA device listing
1200,1201,1201 ADVANCE,1201 ADVANCE EM,1201 CENTER PILLAR,1201 EM,1202 EL,1202 EL ADVANCE,1203 EL,1203 EL…
FDA device listing 1407128208 · TECHNOMED INDIA
Key facts
| Proprietary names | 1200,1201,1201 ADVANCE,1201 ADVANCE EM,1201 CENTER PILLAR,1201 EM,1202 EL,1202 EL ADVANCE,1203 EL,1203 EL ADVANCE,1204,1204 ADVANCE,1204 ADVANCE EM,1204 EM,1207,1208,1208 EM,1209,1211,1212,1215,1301,ARYA K3,AYRA ELECTRIC OT TABLE,AYRA K1,AYRA K2,AYRA K4,AYRA K5,AYRA K6,AYRA OT TABLE,C-ARM SURGICAL TABLE,C-ARM TABLE,ELECTRIC MANUAL SURGICAL TABLE,ELECTRIC + MANUAL TABLE,ELECTRIC OT TABLE,ELECTRIC… |
|---|---|
| Owner/operator | TECHNOMED INDIA |
| Owner/operator number | 10088944 |
| Product codes | GDC |
| Device names | GDC - Table, Operating-Room, Electrical |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4960 |
| Review panels | General & Plastic Surgery |
| Registered establishments | TECHNOMED INDIA |
| Establishment registrations | 3025628903 |
| FEI numbers | 3025628903 |
| Establishment operations | 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