Devices

Device Recall Modular Verres Body/Obturator

Model / Serial
Lot K3
Product Classification
General and Plastic Surgery Devices
Device Class
1
Implanted device?
No
Distribution
US Distribution to the state of : UT
Product Description
Pilling Modular Verres Body/Obturator, Product Code 140880
Manufacturer
Teleflex Medical
1 Event
- Recall of Device Recall Modular Verres Body/Obturator

Manufacturer

Teleflex Medical

Manufacturer Address
Teleflex Medical, 2917 Weck Dr, Research Triangle Park NC 27709-0186
Manufacturer Parent Company (2017)
Teleflex Incorporated
Source
USFDA

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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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