Devices

Anspach eMax 2

Model / Serial
Model: IFU: 18-0047 Revisions A & B, 18-0074 Revision A, 18-0105 Revision A, Affected:
Manufacturer
Anspach Effort Inc
1 Event
- Recall of Anspach eMax 2

Manufacturer

Anspach Effort Inc

Manufacturer Parent Company (2017)
Johnson & Johnson
Source
NZMMDSA

2 devices with a similar name

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Anspach eMax 2 Drill System

Model / Serial
Model: IFU: 18-0047 Revisions A & B, 18-0074 Revision A, 18-0105 Revision A, Affected:
Manufacturer
Anspach Effort Inc

Device Recall Anspach eMax 2 Modified Hand Control

Model / Serial
Part Number: 98-0016; Serial Numbers: 200008201, 200008202, 200008203, 200008204, 200008205, 200008206.
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 98-0016***eMax 2 Modified Hand Control***Rx Only*** || This device is intended to be used with Anspach Systems
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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