Home GUDID 06972624970141 BeneCath®
Primary DI 06972624970141
Brand BeneCath®
Company Hangzhou Jimushi Meditech Co., Ltd.
Model NCW10F
Published 2021-01-01
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 GBM Catheter, Urethral
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class GBM Catheter, Urethral Gastroenterology, Urology 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 06972624970141 Package GS1 30 In Commercial Distribution 26972624970145 Package GS1 10 In Commercial Distribution 16972624970148 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 06972624970141 06972624970141 6972624970141 26972624970145 26972624970145 16972624970148 16972624970148
GMDN Terms# Term, Definition table Term Definition Intermittent urethral drainage catheter, non-antimicrobial, single-use A flexible or rigid tube designed for a single insertion into the urethra, typically by the user (i.e., self-applied), to the urinary bladder to provide urine drainage, typically for an individual who is physiologically incapable of voiding. The device is typically pre-lubricated or coated with/made of materials that facilitate easy insertion and removal [e.g., polytetrafluoroethylene (PTFT) - Teflon, or glass] and is disposed of after use; it does not include an antimicrobial agent(s). The device may be male or female dedicated. This is a single-use device.
Regulatory Flags# DUNS number 413190154 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex true 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 14026704943019 TELEFLEX TELEFLEX INCORPORATED GBM 2026-04-10 14026704943026 TELEFLEX TELEFLEX INCORPORATED GBM 2026-04-10 14026704943033 TELEFLEX TELEFLEX INCORPORATED GBM 2026-04-10 14026704943040 TELEFLEX TELEFLEX INCORPORATED GBM 2026-04-10 14026704943057 TELEFLEX TELEFLEX INCORPORATED GBM 2026-04-10 14026704943125 TELEFLEX TELEFLEX INCORPORATED GBM 2026-04-10 14026704943132 TELEFLEX TELEFLEX INCORPORATED GBM 2026-04-10 14026704943149 TELEFLEX TELEFLEX INCORPORATED GBM 2026-04-10 14026704943170 TELEFLEX TELEFLEX INCORPORATED GBM 2026-04-10 14026704943194 TELEFLEX TELEFLEX INCORPORATED GBM 2026-04-10 14026704943255 TELEFLEX TELEFLEX INCORPORATED GBM 2026-04-10 10192253058437 Dover Cardinal Health 200, LLC GBM 2025-01-23 10192253058444 Dover Cardinal Health 200, LLC GBM 2025-01-23 10192253058451 Dover Cardinal Health 200, LLC GBM 2025-01-23 10192253058468 Dover Cardinal Health 200, LLC GBM 2025-01-23 10192253058475 Dover Cardinal Health 200, LLC GBM 2025-01-23 10192253058482 Dover Cardinal Health 200, LLC GBM 2025-01-23 10192253058499 Dover Cardinal Health 200, LLC GBM 2025-01-23 10192253058505 Dover Cardinal Health 200, LLC GBM 2025-01-23 10192253058512 Dover Cardinal Health 200, LLC GBM 2025-01-23 10192253058529 Dover Cardinal Health 200, LLC GBM 2025-01-23 10192253058536 Dover Cardinal Health 200, LLC GBM 2025-01-23 10192253058543 Dover Cardinal Health 200, LLC GBM 2025-01-23 10192253027761 Dover Cardinal Health 200, LLC GBM 2022-11-08 15390166167122 VaPro Pocket HOLLISTER INCORPORATED GBM 2022-11-01 15390166167139 VaPro Pocket HOLLISTER INCORPORATED GBM 2022-11-01 15390166167146 VaPro Pocket HOLLISTER INCORPORATED GBM 2022-11-01 15390166167153 VaPro Pocket HOLLISTER INCORPORATED GBM 2022-11-01 00610075052967 VaPro Pocket HOLLISTER INCORPORATED GBM 2022-09-30 00610075052974 VaPro Pocket HOLLISTER INCORPORATED GBM 2022-09-30