Devices

Device Recall ASpace SIBD and Arcadius XP L systems

Model / Serial
All Lots
Product Classification
General and Plastic Surgery Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide Distribution: US (nationwide) and country of: Canada.
Product Description
Flexible Drill; || SJ723R; NON STERILE; || B Braun Aesculap; || Aesculap AG || These instruments are intended for use during the implantations of the A-Space SIBD and Arcadius XP L systems.
Manufacturer
Aesculap, Inc.
2 Events
- Recall of Device Recall ASpace SIBD and Arcadius XP L systems
- Recall of Device Recall ASpace SIBD and Arcadius XP L systems

Manufacturer

Aesculap, Inc.

Manufacturer Address
Aesculap, Inc., 3773 Corporate Pkwy, Center Valley PA 18034-8217
Manufacturer Parent Company (2017)
Ludwig G. Braun Gmbh U. Co. Kg
Source
USFDA

One device with a similar name

Learn more about the data here

Device Recall ASpace SIBD and Arcadius XP L systems

Model / Serial
all lots
Product Classification
General and Plastic Surgery Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide Distribution: US (nationwide) and country of: Canada.
Product Description
Flexible Bone Awl; || SJ607R; NON STERILE; || B Braun Aesculap; || Aesculap AG: || These instruments are intended for use during the implantations of the A-Space SIBD and Arcadius XP L systems.
Manufacturer
Aesculap, 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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