Devices

Foot Pedal

Model / Serial
EMAX2-FP Serial Numbers: C26302250301, C26302250302, C26302250303, C26302250304, 5044044307, 31495607, 32380602, 31832209, 31832202 and 32366805; and EPLUS-FP Serial Numbers: C26302200804 , C26302200802, C27302221701 and C08301701901.
Product Classification
Neurological Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution -- Canada, Indonesia, United Kingdom, Korea and United States (NC, OK, TN, CA, KS, MI and WA).
Product Description
Foot Pedal, Foot Control for SC2000 and SC2100 Powered, simple cranial drills, burrs, trephines, and their accessories. Catalog Numbers: EMAX2-FP and FPLUS-FP. || Indicated to cut and shape bone including bones of the spine and cranium.
Manufacturer
The Anspach Effort, Inc.
1 Event
- Recall of Foot Pedal

Manufacturer

The Anspach Effort, Inc.

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

4 devices with a similar name

Learn more about the data here

CUSA Clarity foot pedal packed with CUSA Clarity console

Model / Serial
Product Description
Medical-electromechanical equipment
Manufacturer
Integra LifeSciences (Ireland) Ltd

Device Recall Anspach eMax2 Lower Profile Foot Pedal

Model / Serial
Part Numbers: 98-0002, 98-0004, 98-0007, 98-0030, 98-0036; Serial Numbers: 200245, 20032601, 20032602 20032603, 20032604, 20032504, 20032508, 20032502, 20032503, 20032506, 20032702, 20032701, 20032507, 20032501, 20032505, 200027203, 200027201, 200027202, 200064104.
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***eMax2 Lower Profile Foot Pedal***Rx Only*** || This device is intended to be used with Anspach Systems
Manufacturer
The Anspach Effort, Inc.

Device Recall Aesculap(R) Bipolar Coagulator/Foot Pedal

Model / Serial
Manufacture date on the label on the bottom of the foot pedal - any product with manufactured dates between 45/10 and 31/12
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
USA Nationwide Distribution including the states of: AR, CA, FL, IN, IA, KS, MD, MN, MO, OR, TN, TX, VA and WA.
Product Description
Aesculap Bipolar Generator Foot Pedal, Catalog No. GK226, for electrosurgical cutting and coagulation.
Manufacturer
Aesculap, Inc.

Foot Pedal, Power Cord

Model / Serial
MD0120, MD0140
Product Description
MD: Tissue morcellation system
Manufacturer
Ethicon Inc.

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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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