Home GUDID 00888118108364 DISTRACTION, INTERNAL, STERILE
Primary DI 00888118108364
Brand DISTRACTION, INTERNAL, STERILE
Company KLS-Martin L.P.
Model 51-557-20-81
Device description SIZER, FOR 51-557-15-71 AND 51-557-20-71, POLYAMIDE
Published 2018-09-26
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 HWT TEMPLATE
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class HWT Template Orthopedic 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00888118108364 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 00888118108364 00888118108364 888118108364 0888118108364
GMDN Terms# Term, Definition table Term Definition Surgical implant template, single-use A device designed to determine the appropriate size and placement of a non-dental implant for a patient prior to or during implantation surgery. It is typically available as a graduated set or an individual plate (e.g., a translucent plastic sheet or a cut metal shape) with patterns/sizes corresponding to the size of the implant to be used to aid the surgeon in final selection of implant size, placement, and/or adaption. It is used for, e.g., total- or partial-joint prostheses, bone fracture fixation implants (plates, nails, including skull plate implants) or other types of surgical implants. This is a single-use device.
Device Sizes# Type, Value, Unit table Type Value Unit Device Size Text, specify 0
Regulatory Flags# DUNS number 826499238 Device count 1 DM exempt false Premarket exempt true 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# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00888118108357 DISTRACTION, INTERNAL, STERILE 51-556-20-81 2018-09-26 00888118147226 LEVEL ONE EXTREMITY 26-950-64-04 2026-07-21 00888118147233 LEVEL ONE EXTREMITY 26-950-65-04 2026-07-21 00888118147240 LEVEL ONE EXTREMITY 26-950-66-04 2026-07-21 00888118147257 LEVEL ONE EXTREMITY 26-950-67-04 2026-07-21 00888118147264 LEVEL ONE EXTREMITY 26-950-68-04 2026-07-21 00888118147271 LEVEL ONE EXTREMITY 26-950-69-04 2026-07-21 00888118147714 LEVEL ONE EXTREMITY 26-950-58-04 2026-07-21 00888118147721 LEVEL ONE EXTREMITY 26-950-59-04 2026-07-21 00888118147738 LEVEL ONE EXTREMITY 26-950-62-04 2026-07-21 00888118147745 LEVEL ONE EXTREMITY 26-950-63-04 2026-07-21 00888118154620 LEVEL ONE CMF 25-315-92-91 2026-07-21 00888118154637 LEVEL ONE CMF 50-743-06-09 2026-07-21 00888118154644 LEVEL ONE, STERILE 25-433-97-71 2026-07-21 00888118154651 LEVEL ONE, STERILE 25-438-97-71 2026-07-21 00888118154668 LEVEL ONE, STERILE 25-439-91-71 2026-07-21 00888118154675 LEVEL ONE, STERILE 25-486-97-71 2026-07-21 00888118154682 LEVEL ONE, STERILE 25-487-97-71 2026-07-21 00888118154699 LEVEL ONE, STERILE 50-817-15-71 2026-07-21 00888118154705 LEVEL ONE, STERILE 50-817-20-71 2026-07-21
Other Devices Sharing Product Codes#