FDA device listing
Air Dermatome (DERMATOME-AIR POWERED; Air Dermatome Handpiece; Air Dermatome Hose; Autoclave case; Width…
FDA device listing 1224976064 · JIANGSU MJD MEDICAL TECHNOLOGY CO.,LTD.
Key facts
| Proprietary names | Air Dermatome (DERMATOME-AIR POWERED; Air Dermatome Handpiece; Air Dermatome Hose; Autoclave case; Width Plates;,Autoclave case; Width Plates; Medical Dermatome Blades; Screwdriver; Connection Cord);,Battery Operated Dermatome (DERMATOME-BATTERY OPERATED; Battery Operated Dermatome Handpiece; Battery; Motor; Charger;,Drum Dermatome; Medical Dermatome Blade (Dermatome knife),Electric Dermatome… |
|---|---|
| Owner/operator | JIANGSU MJD MEDICAL TECHNOLOGY CO.,LTD. |
| Owner/operator number | 10084964 |
| Product codes | GFD |
| Device names | GFD - Dermatome |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4820 |
| Review panels | General & Plastic Surgery |
| Registered establishments | JIANGSU MJD MEDICAL TECHNOLOGY CO.,LTD. |
| Establishment registrations | 3023244395 |
| FEI numbers | 3023244395 |
| Establishment operations | 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