Home GUDID 10801902170191 ARROW
Primary DI 10801902170191
Brand ARROW
Company TELEFLEX INCORPORATED
Model IPN917307
Catalog number CS-01701
Published 2026-08-03
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile true
Single use true
Product Codes# Code, Name table Code Name FGE Stents, drains and dilators for the biliary ducts
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 20801902170198 Package GS1 5 In Commercial Distribution 10801902170191 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 20801902170198 20801902170198 10801902170191 10801902170191
GMDN Terms# Term, Definition table Term Definition ERCP catheter, non-balloon, non-electrical, single-use A non-electrical flexible tube inserted through a flexible endoscope, after its placement in the duodenum via the oral cavity, for the endoscopic cannulation of the gastrointestinal ductal system (i.e., the pancreatic, hepatic, and/or common bile ducts) during endoscopic retrograde cholangiopancreatography (ERCP). It is typically a single-lumen device made of radiopaque plastic materials with incremental markings at the distal tip, used to deliver a contrast medium to the ducts for their radiographic visualization; it does not incorporate a balloon. This is a single-use device.
Regulatory Flags# DUNS number 002348191 Device count 1 DM exempt false Premarket exempt true HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label true Expiration date on label true Donation ID number false Contains natural rubber latex true No natural rubber latex false Sterilization required before use false Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 04052838002400 Endoflux™ Medi-Globe GmbH FGE 2026-07-20 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