Home GUDID 23596010191070 BUCK
Primary DI 23596010191070
Brand BUCK
Company Smith & Nephew, Inc.
Model 71279420
Catalog number 71279420
Device description BUCK CEMENT RESTRICTOR SIZE 30MM
Published 2015-08-29
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 LZN CEMENT OBTURATOR
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class LZN Cement Obturator General, Plastic Surgery 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 23596010191070 Package GS1 3 In Commercial Distribution 03596010191076 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 23596010191070 23596010191070 03596010191076 03596010191076 3596010191076
GMDN Terms# Term, Definition table Term Definition Polymer orthopaedic cement restrictor, non-bioabsorbable, sterile A sterile, non-bioabsorbable, implantable device designed to be inserted into the medullary canal of a bone (e.g., femur, tibia, or humerus) during orthopaedic surgery to prevent cement progression in the diaphysis and therefore facilitate cement pressurization during the introduction of an implant. It is typically made of polyetheretherketone (PEEK) or ultrahigh molecular weight polyethylene (UHMWPE) and is available in a variety of designs, e.g., straight or tapered, hollow with a fenestrated surface, and it may have a toothed surface to prevent its migration from the desired location. It may incorporate a metal orientation marker for radiographs and is not intended for spinal indication.
Regulatory Flags# DUNS number 109903521 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 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 03760177046542 CLEARCUT TEKNIMED LZN 2020-11-25 03760177046573 CLEARCUT TEKNIMED LZN 2020-11-25 03760177046603 CLEARCUT TEKNIMED LZN 2020-11-25 03760177046634 CLEARCUT TEKNIMED LZN 2020-11-25 03760177046665 CLEARCUT TEKNIMED LZN 2020-11-25 03760177046696 CLEARCUT TEKNIMED LZN 2020-11-25 03760177046535 CLEARCUT TEKNIMED LZN 2020-09-24 00889024510326 NA Zimmer, Inc. LZN 2018-09-14 00889024510333 NA Zimmer, Inc. LZN 2018-09-14 00889024510340 NA Zimmer, Inc. LZN 2018-09-14 00889024510357 NA Zimmer, Inc. LZN 2018-09-14 00889024510364 NA Zimmer, Inc. LZN 2018-09-14 00889024510371 NA Zimmer, Inc. LZN 2018-09-14 00888912023443 DJO SURGICAL Encore Medical, L.P. LZN 2017-05-04 00888912023450 DJO SURGICAL Encore Medical, L.P. LZN 2017-05-04 00888912023467 DJO SURGICAL Encore Medical, L.P. LZN 2017-05-04 00888912023474 DJO SURGICAL Encore Medical, L.P. LZN 2017-05-04 00888912023481 DJO SURGICAL Encore Medical, L.P. LZN 2017-05-04 00888912073806 DJO SURGICAL Encore Medical, L.P. LZN 2017-05-04 00889024376724 NA Zimmer, Inc. LZN 2016-08-31 00889024376748 NA Zimmer, Inc. LZN 2016-08-31 00889024376755 NA Zimmer, Inc. LZN 2016-08-31 00889024380189 NA Zimmer, Inc. LZN 2016-08-31 00889024432918 NA Zimmer, Inc. LZN 2016-07-15 00889024432970 NA Zimmer, Inc. LZN 2016-05-24 00889024432987 NA Zimmer, Inc. LZN 2016-05-24 00889024432994 NA Zimmer, Inc. LZN 2016-05-24 00889024433007 NA Zimmer, Inc. LZN 2016-05-24 00889024433014 NA Zimmer, Inc. LZN 2016-05-24 00889024433021 NA Zimmer, Inc. LZN 2016-05-24
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