Home GUDID 10195327421649 Medline Industries, Inc.
Primary DI 10195327421649
Brand Medline Industries, Inc.
Company MEDLINE INDUSTRIES, INC.
Model DYNJ901391F
Catalog number DYNJ901391F
Device description IM NAIL
Published 2023-06-04
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 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 10195327421649 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 10195327421649 10195327421649
GMDN Terms# Term, Definition table Term Definition General surgical procedure kit, non-medicated, single-use A typically non-dedicated collection of various surgical instruments, sometimes with dressings and/or other materials, but that does not contain pharmaceuticals, intended to be used during: 1) open abdominal surgery; 2) a range of open surgical procedures across multiple clinical specialties (non-dedicated); 3) non-orthopaedic trauma surgery; 4) minor dermatological surgery; or 5) cosmetic surgery below the head. As a kit that includes procedural devices, it is neither dedicated to surgical scrubbing, surgical patient preparation, nor anaesthesia, and is not a dedicated biopsy kit. This is a single-use device.
Regulatory Flags# DUNS number 025460908 Device count 1 DM exempt false Premarket exempt true HCT/P false Kit true 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 00810220800171 Adler Instrument Company Adler, Inc. MDM 2026-05-26 00810220800188 Adler Instrument Company Adler, Inc. MDM 2026-05-26 06438394002678 Activa Instrument Bioretec Oy MDM 2026-03-23 06438394002685 Activa Instrument Bioretec Oy MDM 2026-03-23 06438394002692 Activa Instrument Bioretec Oy MDM 2026-03-23 06438394020382 Activa Instrument Bioretec Oy MDM 2026-03-23 06438394010956 Activa Instrument Bioretec Oy MDM 2026-03-23 00198506089619 ELMED INCORPORATED ELMED INCORPORATED MDM 2026-03-17 00888867519459 Arthrex® ARTHREX, INC. MDM 2026-03-16 00888867519473 Arthrex® ARTHREX, INC. MDM 2026-03-16 00888867519503 Arthrex® ARTHREX, INC. MDM 2026-03-16 00888867519510 Arthrex® ARTHREX, INC. MDM 2026-03-16 00888867529755 Arthrex® ARTHREX, INC. MDM 2026-03-16 00888867529793 Arthrex® ARTHREX, INC. MDM 2026-03-16 00888867529823 Arthrex® ARTHREX, INC. MDM 2026-03-16 00198506089510 ELMED INCORPORATED ELMED INCORPORATED MDM 2026-03-13 00810158219236 PRINCETON Princeton Medical Group, Inc. MDM 2026-03-12 00810158219243 PRINCETON Princeton Medical Group, Inc. MDM 2026-03-12 00810158219250 PRINCETON Princeton Medical Group, Inc. MDM 2026-03-12 00810158219281 PRINCETON Princeton Medical Group, Inc. MDM 2026-03-12 00810158219304 PRINCETON Princeton Medical Group, Inc. MDM 2026-03-12 00810158219311 PRINCETON Princeton Medical Group, Inc. MDM 2026-03-12 00810158219359 PRINCETON Princeton Medical Group, Inc. MDM 2026-03-12 00810158219373 PRINCETON Princeton Medical Group, Inc. MDM 2026-03-12 00810158219007 PRINCETON Princeton Medical Group, Inc. MDM 2026-03-11 00810158219014 PRINCETON Princeton Medical Group, Inc. MDM 2026-03-11 00810158219021 PRINCETON Princeton Medical Group, Inc. MDM 2026-03-11 00810158219038 PRINCETON Princeton Medical Group, Inc. MDM 2026-03-11 00810158219069 PRINCETON Princeton Medical Group, Inc. MDM 2026-03-11 00810158219090 PRINCETON Princeton Medical Group, Inc. MDM 2026-03-11
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