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WTO notification · TBT

PanamaProposed measure, may since have been adopted

Medical equipment, Laboratory medicine – Panama

Executive Decree regulating Law 90 of 26 December 2017, on Medical Devices and related products and establishing other provisions, amended by Law 92 of 12 September 2019.

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Decreto Ejecutivo Que reglamenta la Ley 90 de 26 de diciembre de 2017, Sobre Dispositivos Médicos y productos afines y dicta otras disposiciones, reformada por la Ley 92 de 12 de septiembre de 2019.

Panama notified this proposed TBT measure to the WTO on 8 December 2025. The comment period closed on 6 February 2026.

Expodite puts notifications like this one in your Updates centre, matched to the HS codes of your products and the markets you export to. Opens the requirements check for Panama in your Expodite account.

Source: WTO ePing (opens in a new tab). Summaries by Expodite, which is independent of the WTO.

Published here:

At a glance

Products

Medical Devices, Biomedical Equipment and In Vitro Diagnostic Medical Devices (DMDIV) and related products

View original

Dispositivos Médicos, Equipos Biomédicos y Dispositivos Médicos de Diagnóstico In Vitro (DMDIV) y productos a fines

Notifying member
Panama
Status
Proposed measure, may since have been adoptedNotified as a draft on 8 December 2025. Check WTO ePing or Panama for its current status.
Objectives
  • Other
Area
TBT: Technical product rulesTechnical barriers to trade
Notification type
Regular notification
Document symbol
G/TBT/N/PAN/135
ICS classification
  • 11.040 Medical equipment
  • 11.100.10 In vitro diagnostic test systems
Keywords
Human health

Key dates

Distributed by the WTO
Comment deadline
Closed on 6 February 2026
Proposed adoption
To be determined
Proposed entry into force
6 months from adoption

How to comment

The comment period closed on 6 February 2026. You can still raise concerns about the measure with your country's WTO TBT enquiry point, quoting the document symbol G/TBT/N/PAN/135; it can take them up with Panama.

Find your country's enquiry point on WTO ePing (opens in a new tab)

What the notification says

The notified document establishes regulations relating to the manufacturing, packaging, importation, exportation, re-exportation, information, advertising, labelling, distribution, marketing, storage, use and final disposal of medical devices in Panama, including in vitro diagnostic medical devices (IVDs).

Sources

Expodite writes its summary from the official record. The notification and the documents it notifies are on the WTO's own websites.

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