Home GUDID 07613327329797 Instrument
Primary DI 07613327329797
Brand Instrument
Company Howmedica Osteonics Corp.
Model I-K2871TS89
Catalog number I-K2871TS89
Device description SPECIALTY TRIATHLON PKR TIBIAL STYLUS SIZE 8 AND 9mm
Published 2021-10-04
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true Product Codes# Code, Name table Code Name JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER MBH PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer Orthopedic 2 MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 07613327329797 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 07613327329797 07613327329797 7613327329797
GMDN Terms# Term, Definition table Term Definition Orthopaedic prosthesis implantation instrument, reusable A hand-held surgical instrument intended to be used during implantation of an orthopaedic prosthesis, either manually or as a computer-assisted surgery (CAS) device, to aid in the navigation/placement of the prosthesis or other instruments. It may be used for the following applications: 1) to hold/align/fix bone preparation instruments, prosthesis, or prosthesis component; 2) to provide relative position landmarks; 3) to ascertain correct spatial orientation or limb alignment; and/or 4) as an interface between prosthesis components. This is a reusable device intended to be sterilized prior to use.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 058311945 Device count 1 Lot or batch true Sterilization required before use true Other Devices From This Company# Other Devices Sharing Product Codes# Primary DI, Brand, Company table Primary DI Brand Company Product code Published 00840097536552 iTotal Identity CR 3DP Porous Restor3d, Inc. MBH 2026-07-31 00840097536552 iTotal Identity CR 3DP Porous Restor3d, Inc. JWH 2026-07-31 00840097536569 iTotal Identity CR 3DP Porous Restor3d, Inc. JWH 2026-07-31 00840097536569 iTotal Identity CR 3DP Porous Restor3d, Inc. MBH 2026-07-31 00840097536576 iTotal Identity CR 3DP Porous Restor3d, Inc. JWH 2026-07-31 00840097536576 iTotal Identity CR 3DP Porous Restor3d, Inc. MBH 2026-07-31 00840097536583 iTotal Identity CR 3DP Porous Restor3d, Inc. JWH 2026-07-31 00840097536583 iTotal Identity CR 3DP Porous Restor3d, Inc. MBH 2026-07-31 00840097536590 iTotal Identity CR 3DP Porous Restor3d, Inc. JWH 2026-07-31 00840097536590 iTotal Identity CR 3DP Porous Restor3d, Inc. MBH 2026-07-31 03701089509695 AMPLITUDE AMPLITUDE SAS JWH 2026-07-31 03701089517492 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517508 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517515 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517522 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517539 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517546 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517553 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517560 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517577 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517584 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517591 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517607 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517614 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517621 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517638 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517645 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517652 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089517669 TRAX AMPLITUDE SAS JWH 2026-07-29 03701089518390 TRAX AMPLITUDE SAS JWH 2026-07-29