Devices

Device Recall Tumark Q

Model / Serial
Lot numbers: 47883, 47910 & 47911
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
Yes
Distribution
NY - Only one US distributor
Product Description
TUMARK Q, Length 12 cm, Diameter 18G, GTIN 04250195603081, REF 271500, STERILE
Manufacturer
Somatex Medical Technologies GmbH
1 Event
- Recall of Device Recall Tumark Q

Manufacturer

Somatex Medical Technologies GmbH

Manufacturer Address
Somatex Medical Technologies GmbH, Rheinstr. 7 d, Teltow Germany
Manufacturer Parent Company (2017)
E-Med Solutions Gmbh
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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