International Medical Devices Database

Manufacturer Address
MAQUET Inc., 1140 Us Highway 22 Ste 202, Bridgewater NJ 08807-2958
Manufacturer Parent Company (2017)
Getinge AB
Source
USFDA
9 Events

9 devices in the database

XTEN LED DF cupola

Model / Serial
Part Number: 567815999.
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution.
Product Description
XTEN LED DF cupola, P/N: 567815999. || Intended to provide visible illumination for the surgical field or for the examination of the patient.

XTEN LED Video DF cupola

Model / Serial
Part Number: 567801999
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution.
Product Description
XTEN LED Video DF cupola, P/N: 567801999. || Intended to provide visible illumination for the surgical field or for the examination of the patient.

XTEN DF cupola

Model / Serial
Part Number: 567800999
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution.
Product Description
XTEN DF cupola, P/N: 567800999. || Intended to provide visible illumination for the surgical field or for the examination of the patient.

HANAULUX 20042005 TV Spring Arm

Model / Serial
Part Number: 569002998; all serial numbers
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution.
Product Description
HANAULUX 2004-2005 TV Spring Arm, P/N: 569002998. || Intended to provide visible illumination for the surgical field or for the examination of the patient.

HANAULUX 2005 IXL cupola

Model / Serial
Part Number: 56076869, all serial numbers
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution.
Product Description
HANAULUX 2005 IXL cupola, P/N: 56076869. || Intended to provide visible illumination for the surgical field or for the examination of the patient.

4 more

6 manufacturers with a similar name

Learn more about the data here

MAQUET Inc.

Manufacturer Address
MAQUET Inc., 1140 US Highway 22, Bridgewater NJ 08807-2958
Source
USFDA

MAQUET Inc.

Manufacturer Parent Company (2017)
Getinge AB
Manufacturers representative
Gulf Medical Co.
Source
SFDA

Maquet Inc.

Manufacturer Address
Maquet Inc., 45 Barbour Pond Drive, Wayne NJ 07470
Manufacturer Parent Company (2017)
Getinge AB
Source
USFDA

MAQUET Inc.

Manufacturer Address
MAQUET Inc., 1140 US Highway 22 East, Suite 202, Bridgewater NJ 08807-2958
Manufacturer Parent Company (2017)
Getinge AB
Source
USFDA

MAQUET Inc.

Manufacturer Address
MAQUET Inc., 45 Barbour Pond Drive, Wayne NJ 07470
Manufacturer Parent Company (2017)
Getinge AB
Source
USFDA

One more

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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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