International Medical Devices Database

Manufacturer Parent Company (2017)
Handicare Group Ab
Source
NZMMDSA
1 Event
- Recall of Handicare System RoMedic ReTurn 7400 and 7500 Patient Transfer device

One device in the database

Handicare System RoMedic ReTurn 7400 and 7500 Patient Transfer device

Model / Serial
Model: Models 7400 and 7500, Affected: Manufactured between Apr-2009 and May 2011

14 manufacturers with a similar name

Learn more about the data here

HANDICARE AB

Manufacturer Parent Company (2017)
Handicare Group Ab
Source
MSHM

Handicare AB

Manufacturer Address
Handicare AB, Maskinvagen 17, Lulea Sweden
Manufacturer Parent Company (2017)
Handicare Group Ab
Source
USFDA

Handicare AB

Manufacturer Parent Company (2017)
Handicare Group Ab
Source
AEMPSVFOI

Handicare AB

Manufacturer Parent Company (2017)
Handicare Group Ab
Manufacturers representative
Al Safwa Dimensions
Source
SFDA

Handicare AB

Manufacturer Parent Company (2017)
Handicare Group Ab
Source
BAM

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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