Home GUDID 10885862013750 NA
Primary DI 10885862013750
Brand NA
Company Exactech, Inc.
Model 105-02-45
Catalog number 105-02-45
Device description DRILL GUIDE, 4.5mm
Published 2022-09-20
Public version status Update
Distribution status Not in Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile false
Single use false Product Codes# Code, Name table Code Name HWC Screw, fixation, bone JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED MBH PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class HWC Screw, Fixation, Bone Orthopedic 2 JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented Orthopedic 2 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer Orthopedic 2 LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented 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 10885862013750 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 10885862013750 10885862013750
GMDN Terms# Term, Definition table Term Definition Surgical guillotine A manually-operated surgical instrument designed to cut body tissues and/or organs by using a sliding blade during a surgical intervention. It typically consists of a metal frame through which runs the sliding blade which is moved by the device operator with a handcrank mechanism. It is made of high-grade stainless steel and is available in various shapes and sizes depending on the tissue each is intended to cut. This is a reusable device.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 157565946 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 false Donation ID number false Contains natural rubber latex false No natural rubber latex false 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 00840097536705 Identity CR KA Restor3d, Inc. JWH 2026-09-25 00840097536712 Identity CR KA Restor3d, Inc. JWH 2026-09-25 00840097536729 Identity CR KA 3DP Porous Restor3d, Inc. JWH 2026-09-25 00840097536729 Identity CR KA 3DP Porous Restor3d, Inc. MBH 2026-09-25 00840097536736 Identity CR KA 3DP Porous Restor3d, Inc. JWH 2026-09-25 00840097536736 Identity CR KA 3DP Porous Restor3d, Inc. MBH 2026-09-25 00840097536743 Identity CR KA 3DP Porous Restor3d, Inc. JWH 2026-09-25 00840097536743 Identity CR KA 3DP Porous Restor3d, Inc. MBH 2026-09-25 00840097536750 Identity CR KA 3DP Porous Restor3d, Inc. JWH 2026-09-25 00840097536750 Identity CR KA 3DP Porous Restor3d, Inc. MBH 2026-09-25 00840097536767 Identity CR KA 3DP Porous Restor3d, Inc. JWH 2026-09-25 00840097536767 Identity CR KA 3DP Porous Restor3d, Inc. MBH 2026-09-25 00840097536774 Identity CR KA 3DP Porous Restor3d, Inc. JWH 2026-09-25 00840097536774 Identity CR KA 3DP Porous Restor3d, Inc. MBH 2026-09-25 00840097536781 Identity CR KA Restor3d, Inc. JWH 2026-09-25 00840097536798 Identity CR KA Restor3d, Inc. JWH 2026-09-25 00840097536804 Identity CR KA 3DP Porous Restor3d, Inc. JWH 2026-09-25 00840097536804 Identity CR KA 3DP Porous Restor3d, Inc. MBH 2026-09-25 00840097536811 Identity CR KA 3DP Porous Restor3d, Inc. JWH 2026-09-25 00840097536811 Identity CR KA 3DP Porous Restor3d, Inc. MBH 2026-09-25 00842188131615 CannCompScrew 5.5 (Ti) Trimed, INC. HWC 2026-09-25 00842188131639 CannCompScrew 5.5 (Ti) Trimed, INC. HWC 2026-09-25 00842188131653 CannCompScrew 5.5 (Ti) Trimed, INC. HWC 2026-09-25 00842188131677 CannCompScrew 5.5 (Ti) Trimed, INC. HWC 2026-09-25 00842188131721 CannCompScrew 5.5 (Ti) Trimed, INC. HWC 2026-09-25 00889095401820 ANTHEM GLOBUS MEDICAL, INC. HWC 2026-09-25 00889095401844 ANTHEM GLOBUS MEDICAL, INC. HWC 2026-09-25 00889095401868 ANTHEM GLOBUS MEDICAL, INC. HWC 2026-09-25 00889095401882 ANTHEM GLOBUS MEDICAL, INC. HWC 2026-09-25 00889095401905 ANTHEM GLOBUS MEDICAL, INC. HWC 2026-09-25