Devices

eMax2 PLUS

Model / Serial
All product shipped prior to 09/27/2016; DFU 18-0085; Part No. EMAX2PLUS.
Product Classification
Neurological Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - US Nationwide in the states of HI, DC including PR and the countries of Guam and Japan
Product Description
eMax2 PLUS || Product Usage: || Electric system
Manufacturer
The Anspach Effort, Inc.
1 Event
- Recall of eMax2 PLUS

Manufacturer

The Anspach Effort, Inc.

Manufacturer Address
The Anspach Effort, Inc., 4500 Riverside Dr, Palm Beach Gardens FL 33410-4235
Manufacturer Parent Company (2017)
Johnson & Johnson
Source
USFDA

3 devices with a similar name

Learn more about the data here

Anspach eMax2 and eMax2 Plus Surgical Motor Pedal

Model / Serial
Product Description
medical_device
Manufacturer
Synthes

Device Recall Anspach Custom Device eMax2 Plus Hand Control

Model / Serial
Part Number: 98-0062; Serial Number: E15200088401.
Product Classification
Neurological Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - USA including AL, CA, FL, IA, IL, KY, MN, MS, NC, OH, OK, PA, TN, TX.and Internationally to Canada, Japan, Hungary, Korea and Sweden. .
Product Description
ANSPACH***REF-98-0062***Custom Device eMax2 Plus Hand Control***Rx Only*** || This device is intended to be used with Anspach Systems
Manufacturer
The Anspach Effort, Inc.

Console, eMax2 Plus

Model / Serial
All product shipped prior to 09/27/2016; DFU 18-0085; Part No. SC2100.
Product Classification
General and Plastic Surgery Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide Distribution - US Nationwide in the states of HI, DC including PR and the countries of Guam and Japan
Product Description
Console, eMax2 Plus || Product Usage: || Electric system
Manufacturer
The Anspach Effort, Inc.

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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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