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Global Health Technology AS

Norway NO-MF-000007974 Last updated 21 Oct 2026

Devices
5
Registries
EUDAMED
FDA recalls
0

Catalogue5

About

Global Health Technology's products offers ground breaking solutions within stoma care and wound treatment

From the manufacturer's own website, in their original language. Source

What Global Health Technology AS makes

Global Health Technology AS manufactures the Erland Care series, a line of Class I medical devices designed for patient care and monitoring. These devices are intended for use in clinical and home settings, focusing on non-invasive or low-risk applications such as vital sign monitoring or assistive care solutions.

The company’s portfolio is regulated under EU medical device directives and is listed in the EUDAMED database. The devices fall under Class I classification, indicating minimal risk and compliance with essential requirements for general medical devices. The manufacturer is based in Norway.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Global Health Technology AS manufacture?

Global Health Technology AS specializes in the Erland Care series, a collection of Class I medical devices. These devices are primarily designed for patient care and monitoring, including non-invasive or low-risk applications such as vital sign tracking or assistive solutions. The portfolio is tailored for both clinical and home use environments.

Where is Global Health Technology AS based?

Global Health Technology AS is headquartered in Norway. The company’s location influences its regulatory compliance, particularly under EU medical device directives, which govern its product development and market authorization processes.

Which regulatory registries list Global Health Technology AS’s devices?

Global Health Technology AS’s devices are listed in the EUDAMED database, which is the European Union’s medical device registry. This inclusion ensures transparency and compliance tracking for Class I devices under EU regulations.

How are Global Health Technology AS’s devices classified?

Global Health Technology AS’s devices fall under Class I classification, the lowest risk category for medical devices in the EU. This classification applies because the devices are designed for minimal-risk applications, such as non-invasive monitoring or assistive care, and meet essential requirements for general medical devices without requiring additional conformity assessments.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Norway(from SRN)
Address
107-111, Løkkeveien , Stavanger, Norway
Phone
+47 51 22 55 70
PRRC contact
Victor Manuel Jáuregui Balderrama
EUDAMED SRN
NO-MF-000007974