Home GUDID 00821684014066
IntraStent LD Mega
Primary DI 00821684014066
Brand IntraStent LD Mega
Company Covidien LP
Model S17-26
Device description Large Diameter Biliary Stent
Published 2015-10-09
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
Sterile true
Single use true
Product Codes# Code, Name table Code Name FGE CATHETER, BILIARY, DIAGNOSTIC
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class FGE Stents, Drains And Dilators For The Biliary Ducts Gastroenterology, Urology 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00821684014066 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00821684014066 00821684014066 821684014066 0821684014066
GMDN Terms# Term, Definition table Term Definition Multiple peripheral artery stent, bare-metal A sterile non-bioabsorbable tubular device intended to be alternatively implanted in more than one peripheral artery (e.g., iliac, carotid, renal) to indefinitely maintain patency and improve luminal diameter in patients with atherosclerotic disease or following the recanalization of a total occlusion. It is typically implanted by a dedicated instrument where it self-expands upon release or is balloon expanded. It is made of metal [e.g., nickel-titanium alloy (Nitinol)] and may be a continuous tube of a certain length, a mesh structure, or other design for supporting constant blood flow through the artery. Some types may be used in the biliary duct as a secondary intended use.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0 Length 26 Millimeter
Storage And Handling# Type, Low, High table Type Low High Condition Special Storage Condition, Specify 0 0 ;
Regulatory Flags# DUNS number 968903703 Device count 1 Lot or batch true Expiration date on label true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 06959664925645 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-06-18 06959664925676 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-06-18 06959664925584 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664925614 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664925959 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664925980 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664926017 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664926048 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664926314 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664926345 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664926376 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664926406 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664926673 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664926703 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664926734 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664926765 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664927038 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664927069 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664927090 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664927120 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664927403 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664927434 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664927465 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664927496 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664928943 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664928974 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664929001 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664929032 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664929070 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15 06959664929100 NA Hangzhou AGS MedTech Co., Ltd. FGE 2026-04-15