Home GUDID 08033390301312 Lock Bipolar Femoral Head
Primary DI 08033390301312
Brand Lock Bipolar Femoral Head
Company LIMACORPORATE SPA
Model 9055.27.010
Catalog number 9055.27.010
Device description Lock Bipolar Femoral Head - Pusher Liner
Published 2025-06-10
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true Product Codes# Code, Name table Code Name JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented KWZ Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented Orthopedic 2 KWY Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented Orthopedic 2 KWZ Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer Orthopedic 2 LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 08033390301312 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 08033390301312 08033390301312 8033390301312
GMDN Terms# Term, Definition table Term Definition Orthopaedic implant driver A hand-held manual surgical instrument designed to impart force to an orthopaedic implantable device that is inserted to fix or fasten together bones. The device is frequently used to insert devices such as screws, nails, plates, or wires that are used to fix fractured or damaged bones and/or to attach orthopaedic prostheses to the bones. It is typically made of high-grade stainless steel or titanium (Ti). This is a reusable device.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 432066322 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 05056139247293 Icona Hip Stem CORIN LTD KWY 2025-04-07 10885862015181 Aura Exactech, Inc. JDI 2022-10-04 10885862015198 Aura Exactech, Inc. JDI 2022-10-04 10885862015204 Aura Exactech, Inc. JDI 2022-10-04 10885862015211 Aura Exactech, Inc. JDI 2022-10-04 10885862013743 NA Exactech, Inc. JDI 2022-09-20 10885862013743 NA Exactech, Inc. LPH 2022-09-20 10885862013750 NA Exactech, Inc. LPH 2022-09-20 10885862013750 NA Exactech, Inc. JDI 2022-09-20 10885862022448 NA Exactech, Inc. JDI 2022-09-19 10885862022448 NA Exactech, Inc. LPH 2022-09-19 10885862022455 NA Exactech, Inc. LPH 2022-09-19 10885862022455 NA Exactech, Inc. JDI 2022-09-19 10885862029867 NA Exactech, Inc. LPH 2022-09-19 10885862029867 NA Exactech, Inc. JDI 2022-09-19 10885862033598 Novation Exactech, Inc. JDI 2022-08-25 10885862033604 Novation Exactech, Inc. JDI 2022-08-25 10885862033611 Novation Exactech, Inc. JDI 2022-08-25 10885862033628 Novation Exactech, Inc. JDI 2022-08-25 10885862033635 Novation Exactech, Inc. JDI 2022-08-25 10885862033642 Novation Exactech, Inc. JDI 2022-08-25 10885862033741 Novation Exactech, Inc. JDI 2022-08-25 10885862010551 NA Exactech, Inc. LPH 2022-08-18 10885862010551 NA Exactech, Inc. JDI 2022-08-18 10885862010575 NA Exactech, Inc. LPH 2022-08-18 10885862010575 NA Exactech, Inc. JDI 2022-08-18 10885862010582 NA Exactech, Inc. JDI 2022-08-18 10885862010582 NA Exactech, Inc. LPH 2022-08-18 10885862010872 NA Exactech, Inc. JDI 2022-08-18 10885862010872 NA Exactech, Inc. LPH 2022-08-18