Devices

Device Recall Stent Delivery Catheter

Model / Serial
Device Codes: S-04-120-120-G3 (Lot Number 05180062); S-04-040-120-G3 (Lot Numbers 05180031); S-04-060-120-G3 (Lot Number 05187032); S-05-040-120-G3 (Lot Number 05180034); S-05-060-120-G3 (Lot Number 05180035); S-05-080-120-G3 (Lot Number 05180036); S-05-100-120-G3 (Lot Number 05180037); and S-06-080-120-G3 (Lot Number 05180042).
Product Classification
Gastroenterology-Urology Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide Distribution-USA (nationwide) including the states of AL, IL, NJ, NV, and PA.
Product Description
SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent Transhepatic Biliary System. || Intended to be used for palliative treatment of biliary strictures produced by malignant neoplasms.
Manufacturer
Idev Technologies, Inc.
1 Event
- Recall of Device Recall Stent Delivery Catheter

Manufacturer

Idev Technologies, Inc.

Manufacturer Address
Idev Technologies, Inc., 253 Medical Center Blvd, Webster TX 77598
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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