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SafeR Syringe and SafeR Sting
FDA 510(k)EUDAMEDClass II (US FDA 510(k))
510(k) K221981
Identifiers
- 510(k) Number
- K221981 FDA 510(k)
- FDA Product Code
- MEG FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 880.5860 FDA 510(k)
- Regulation Number
- 880.5860 FDA 510(k)
- Advisory Committee
- General Hospital FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
SafeR Syringe and SafeR Sting by Roncadelle Operations Srl — Class II — MDR, FDA_510K — listed in FDA 510(k), EUDAMED — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
MDR
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Active |
| FDA 510(k) | United States | FDA_510K | K221981 | Class II | Active |
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Manufacturer
- Manufacturer
- Roncadelle Operations Srl
Sources (2)
- FDA 510(k) K221981 24 fields · synced Jun 20, 2026
- EUDAMED 1 fields · synced May 18, 2026