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ANMAT Disposición

Disposición 2319/2002

Manufacturing and Import Authorization Requirements
ArgentinaANMATRegistrationEffective May 9, 2002
What this code is

Disposición 2319/2002 is the official ANMAT identifier for “Manufacturing and Import Authorization Requirements”. Disposición 2319/2002 is the official identifier ANMAT uses for this instrument.

Instrument
Disposición
Full name
Disposición 2319/2002
Category
Registration
Source links
Authority source
Spanish
Authority publication; confirm whether a later amendment or consolidated version applies.
Readable HTML
4 articles · 1 language version
Direct citations can link to an article, for example /data/regulations/argentina/disp-2319-2002.es.html#art-1.
Dates
Published
May 9, 2002
Effective
May 9, 2002
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Each version has stable article anchors for direct citations and highlighting. The readable text is generated from an authority source and does not replace the legally controlling publication.

About this regulation

Manufacturing and Import Authorization Requirements

Governs manufacturing and import authorizations for medical devices. The published official text is the 2004 texto ordenado (Disposición 3433/2004) of Disposición 2319/2002.

Disposición 2319/2002 is the official identifier ANMAT uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.