Pure Global AI
ARSA DDM-F-008

DDM-F-008

Notificación de tecnovigilancia para la industria
HondurasAgencia de Regulación SanitariaVigilanceCurrentness under review
Official source linked
Document status

Currentness under review. Whether this instrument remains applicable is under review. Consult the later instruments and source context below before relying on it.

What this code is

DDM-F-008 is the official ARSA identifier for “Notificación de tecnovigilancia para la industria”. DDM-F-008 is the official identifier ARSA uses for this instrument.

Instrument
DDM-F-008
Full name
DDM-F-008
Category
Vigilance
Source links
Source publication
Spanish
Open the source text
Linked source text; confirm the publisher, publication details and any later amendment or consolidated version.
Readable HTML
1 language version
Read the full text →
Direct citations can link to a specific article or section by appending its fragment identifier.
Dates
Published
—
Effective
—
Readable full text

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.

Spanish full textSpanish — original textRead HTML →
About this regulation

Notificación de tecnovigilancia para la industria

Official ARSA industry form DDM-F-008, version 1, for reporting adverse events and incidents associated with medical devices. Covers initial, follow-up and final reports, device details, patient outcomes and field safety corrective actions.

DDM-F-008 is the official identifier ARSA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.

Source linked