International Medical Devices Database

Manufacturer Parent Company (2017)
Johnson & Johnson
Source
NZMMDSA
1 Event
- Recall of Codman/Micrus NeuroPath Guide Catheters, 6Fr x 100cm

One device in the database

Codman/Micrus NeuroPath Guide Catheters, 6Fr x 100cm

Model / Serial
Model: Models: GST61000000, GMC61000000, Affected: All lots within expiry dating

4 manufacturers with a similar name

Learn more about the data here

Micrus Endovascular Corp.

Manufacturer Parent Company (2017)
Johnson & Johnson
Source
BAM

MICRUS ENDOVASCULAR CORPORATION

Manufacturer Address
SAN JOSE
Manufacturer Parent Company (2017)
Johnson & Johnson
Source
HC

Micrus Endovascular Corporation

Manufacturer Address
Micrus Endovascular Corporation, 821 Fox Lane, San Jose CA 95131
Source
USFDA

Micrus Endovascular Corp., 821 Fox Lane, San Jose, CA 95131

Manufacturer Address
Micrus Endovascular Corp., 821 Fox Lane, San Jose, CA 95131, 821 Fox Ln, San Jose CA 95131-1601
Manufacturer Parent Company (2017)
Johnson & Johnson
Source
USFDA

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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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