Home GUDID 00845854025317 HYPERFLEX
Primary DI 00845854025317
Brand HYPERFLEX
Company Conmed Corporation
Model 8571
Catalog number 8571
Device description 1.6 X 229MM (.062 IN X 9IN) HYPERFLEX NITINOL GUIDE WIRE
Published 2021-10-11
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile false
Single use false Product Codes# Code, Name table Code Name HXB PROBE LXH Orthopedic manual surgical instrument
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class HXB Probe Orthopedic 1 LXH Orthopedic Manual Surgical Instrument Orthopedic 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 20845854025311 Direct Marking GS1 0 10845854025314 Primary GS1 0 00845854025317 Unit of Use GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 20845854025311 20845854025311 10845854025314 10845854025314 00845854025317 00845854025317 845854025317 0845854025317
GMDN Terms# Term, Definition table Term Definition Electrical-only medical device connection cable, reusable A non-patient-contact, insulated, electrical cord with a connector (plug) at both ends designed to transmit electrical power and/or signal (data) between medical devices (e.g., to connect a lead, electrical catheter, handpiece, or monitor to a parent device). It is not intended to connect directly to patient-worn electrodes (i.e., it is not a lead), is not intended to connect to the mains (i.e., not a mains power cable), does not generate any type of power and/or signal, and has no additional non-electrical conducting or processing functionality. This is a reusable device.
Regulatory Flags# DUNS number 071595540 Device count 5 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 true Expiration date on label false Donation ID number false Contains natural rubber latex false 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 00888867550292 Arthrex® ARTHREX, INC. LXH 2026-09-18 00888867550308 Arthrex® ARTHREX, INC. LXH 2026-09-18 00888867550315 Arthrex® ARTHREX, INC. LXH 2026-09-18 00888867550322 Arthrex® ARTHREX, INC. LXH 2026-09-18 00888867550339 Arthrex® ARTHREX, INC. LXH 2026-09-18 00888867550346 Arthrex® ARTHREX, INC. LXH 2026-09-18 00888867550353 Arthrex® ARTHREX, INC. LXH 2026-09-18 00888867550360 Arthrex® ARTHREX, INC. LXH 2026-09-18 00888867550377 Arthrex® ARTHREX, INC. LXH 2026-09-18 00888867550384 Arthrex® ARTHREX, INC. LXH 2026-09-18 00888867552692 Arthrex® ARTHREX, INC. LXH 2026-09-18 00888867552708 Arthrex® ARTHREX, INC. LXH 2026-09-18 00888867552715 Arthrex® ARTHREX, INC. LXH 2026-09-18 00888867552722 Arthrex® ARTHREX, INC. LXH 2026-09-18 00888867552739 Arthrex® ARTHREX, INC. LXH 2026-09-18 00888867552746 Arthrex® ARTHREX, INC. LXH 2026-09-18 00888867552753 Arthrex® ARTHREX, INC. LXH 2026-09-18 00888867552760 Arthrex® ARTHREX, INC. LXH 2026-09-18 00888867574564 Arthrex® ARTHREX, INC. LXH 2026-09-18 00888867574571 Arthrex® ARTHREX, INC. LXH 2026-09-18 00888867574588 Arthrex® ARTHREX, INC. LXH 2026-09-18 04054896000831 Control Gauges Silony Medical GmbH LXH 2026-09-18 04054896000855 Implant Modifier Silony Medical GmbH LXH 2026-09-18 04054896000862 Implant Modifier Silony Medical GmbH LXH 2026-09-18 04054896000879 Implant Modifier Silony Medical GmbH LXH 2026-09-18 04054896000886 Forceps and Clamps Silony Medical GmbH LXH 2026-09-18 04054896000893 (Re-) Positioning Tools Silony Medical GmbH LXH 2026-09-18 04054896000909 (Re-) Positioning Tools Silony Medical GmbH LXH 2026-09-18 04054896000916 (Re-) Positioning Tools Silony Medical GmbH LXH 2026-09-18 04054896000923 Adapter Silony Medical GmbH LXH 2026-09-18
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