Home GUDID 50885403076051 Denver
Primary DI 50885403076051
Brand Denver
Company CAREFUSION 2200, INC
Model 42-3100
Catalog number 42-3100
Device description Denver Tunneler 18FR
Published 2018-07-18
Public version status Update
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 MDM INSTRUMENT, MANUAL, SURGICAL, GENERAL USE
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class MDM Instrument, Manual, Surgical, General Use General, Plastic Surgery 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 50885403076051 Package GS1 10 In Commercial Distribution 10885403076053 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 50885403076051 50885403076051 10885403076053 10885403076053
GMDN Terms# Term, Definition table Term Definition Subcutaneous tunneller, single-use A sterile, hand-held manual surgical instrument designed to create a subcutaneous tunnel (artificial passageway) between percutaneous entry and exit incisions for the subcutaneous placement of a device (e.g., catheter for medication administration, shunt). It is available in a variety of forms and may be: 1) a luminal sheath with a removable inner obturator, intended for co-axial device introduction, followed by sheath removal; or 2) a non-luminal device intended to either lead or pull the device through subcutaneous tissue. It is not intended for tunnelling through deep tissues. This is a single-use device.
Regulatory Flags# DUNS number 832696038 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 false Expiration date on label true 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 10888277688988 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-27 10888277689190 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-27 10888277689206 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-27 10888277689213 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-27 10888277689220 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-27 10888277689237 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-27 10888277689244 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-27 20888277688978 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-27 10080196320899 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-25 10080196321407 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-25 10080196321414 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-25 10080196321438 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-25 10080196321452 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-25 10080196321469 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-25 10080196321476 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-25 10080196321483 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-25 10080196321490 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-25 10888277689183 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-25 10080196321445 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-24 00190776431587 Millennium Avalign Technologies, Inc. MDM 2026-09-22 00850088713886 PRINCETON Princeton Medical Group, Inc. MDM 2026-09-22 00850088713893 PRINCETON Princeton Medical Group, Inc. MDM 2026-09-22 00888867574489 Arthrex® ARTHREX, INC. MDM 2026-09-18 00888867574496 Arthrex® ARTHREX, INC. MDM 2026-09-18 00888867574502 Arthrex® ARTHREX, INC. MDM 2026-09-18 00888867574519 Arthrex® ARTHREX, INC. MDM 2026-09-18 00888867574526 Arthrex® ARTHREX, INC. MDM 2026-09-18 00888867574533 Arthrex® ARTHREX, INC. MDM 2026-09-18 10888277688896 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-18 10888277688902 MEDLINE MEDLINE INDUSTRIES, INC. MDM 2026-09-18
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