Roadrunnerfoot Engineering srl
IT-MF-000008242 · Italy · Milano
Roadrunnerfoot Engineering srl is registered in the European database on medical devices as a manufacturer, with 334 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 334 |
|---|
Most frequent device types declared: SIZE 14,16,18,20,22,23,24,25,26,27,28,29,30 SIDE RIGHT/LEFT, SIZE 16,20,24,26,28,32,38,44 TYPE WITHOUT LOCK AND WITH MATRIX AND LOC, SIZE 22,23,24,25,26,27,28 SIDE RIGHT/LEFT, SIZE 22,23,24,25,26,27,28,29 SIDE RIGHT/LEFT, SIZE I,II,III,IV,V,V-LONG,VI CATEGORY SOFT/HARD.
Devices declared under this manufacturer
- BIMODULAR CLUTCH LOCK PIN INCLUDED
- DYNAMIC PLUS FOOT SIZE VI SOFT
- EQUILIBRIUM FOOT SIZE V SOFT
- LINERS FOR BELOW KNEE AMPUTEE WITH MATRIX AND LOCK SIZE S
- POLYCENTRIC KNEE JOINT COMPACT TITANIUM
- POLYCENTRIC KNEE JOINT WITH SPRING TITANIUM
- ROADFLEXION FOOT HP SIZE V HARD
- SILICONE LINER FOR ABOVE KNEE AMPUTEE WITHOUT LOCK SIZE 24
- SINGLE AXIS FOOT TWO HOLE WITH ADAPTER SIZE 22 LEFT
- STUMP SHOCK ABSORBER SIZE XL
- THREE PRONGS SOCKET ADAPTER MALE
- WALKING FOOT MP SIZE I HARD
Showing 12 of 334 declared devices.
Catalogue references include 1.003.02.V.S, 1.007.02.22L, 1.008.01.VI.S, 3.001.01.BK.MLK.S, 4.001.01.XL, 5.004.05.
European nomenclature codes declared: Y062499.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | ROADRUNNERFOOT ENGINEERING SRL (IT) · FDA 3009307835 |
| Devices in EUDAMED | 334 |
| Country of registration | Italy |
Device-level evidence
| Devices with a numeric GTIN | 334 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: United States only. Roadrunnerfoot Engineering srl is registered in the United States but was not found in the Canadian register.