DDM-F-007
Currentness under review. Whether this instrument remains applicable is under review. Consult the later instruments and source context below before relying on it.
DDM-F-007 is the official ARSA identifier for “Notificación de tecnovigilancia para usuarios”. DDM-F-007 is the official identifier ARSA uses for this instrument.
- Instrument
- DDM-F-007
- Full name
- DDM-F-007
- Category
- Vigilance
- Source publication
- Spanish
- Readable HTML
- 1 language version
- Published
- —
- Effective
- —
Open a language version
Each version has stable passage anchors for direct citations and highlighting. The readable text is generated from an authority source and does not replace the legally controlling publication.
Notificación de tecnovigilancia para usuarios
Official ARSA patient and user form DDM-F-007, version 1, for reporting adverse events and incidents associated with medical devices. Includes notifier and patient details, the incident and its consequences, device identification and signature fields.
DDM-F-007 is the official identifier ARSA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.