International Medical Devices Database

Manufacturer Address
OriGen Biomedical, Inc., 7000 Burleson Rd, Bldg D, Austin TX 78744-3202
Manufacturer Parent Company (2017)
Origen Biomedical Inc.
Source
USFDA
1 Event
- Recall of Device Recall Dual Lumen Catheter

One device in the database

Device Recall Dual Lumen Catheter

Model / Serial
Lot N18549
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution: US (nationwide) and countries of: Spain, UK, Germany, Sweden, and Netherlands.
Product Description
OriGen BIOMEDICAL VV13F Reinforced Dual Lumen Catheter STERILE DISPOSABLE: DO NOT RE-USE Manufactured by: OriGen Biomedical. || OriGene VV13F Reinforced Dual Lumen Catheter indicated for use as a single cannula for both venous drainage and re-infusion of blood in the internal jugular vein during extracorporeal life support procedures of six hours or less.

One manufacturer with a similar name

Learn more about the data here

OriGen Biomedical, Inc.

Manufacturer Address
OriGen Biomedical, Inc., 7000 Burleson Rd Bldg D, Austin TX 78744-3202
Manufacturer Parent Company (2017)
Origen Biomedical Inc.
Source
USFDA

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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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