Home GUDID H679031157510
VA-LCP
Primary DI H679031157510
Brand VA-LCP
Company Synthes GmbH
Model 03.115.751
Catalog number 03115751
Device description SIZING TEMPLATE F/2.4MM VA-LCP VOLAR RIM DSTL RAD PL/6H HD/L
Published 2015-09-14
Public version status Update
Distribution status 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
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class HWC Screw, Fixation, Bone Orthopedic 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 07611819453449 Direct Marking GS1 0 10886982073082 Primary GS1 0 H679031157510 Secondary HIBCC 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 07611819453449 07611819453449 7611819453449 10886982073082 10886982073082
GMDN Terms# Term, Definition table Term Definition Surgical implant template, reusable 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 reusable device.
Sterilization Methods# Method table Method Moist Heat or Steam Sterilization
Regulatory Flags# DUNS number 486711679 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 03700569658212 Xpert PFP NEWCLIP TECHNICS HWC 2026-06-03 00842188131981 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188131998 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132001 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132018 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132025 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132032 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132049 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132056 CannCompScrew 2.0mm (SelfDrill) Trimed, INC. HWC 2026-06-02 00842188132063 Tools - HCS Trimed, INC. HWC 2026-06-02 00842188132070 Tools - HCS Trimed, INC. HWC 2026-06-02 07630894829819 APTUS Medartis AG HWC 2026-06-01 07630894829826 APTUS Medartis AG HWC 2026-06-01 07630894829833 APTUS Medartis AG HWC 2026-06-01 07630894829840 APTUS Medartis AG HWC 2026-06-01 07630894829857 APTUS Medartis AG HWC 2026-06-01 07630894829864 APTUS Medartis AG HWC 2026-06-01 07630894829871 APTUS Medartis AG HWC 2026-06-01 07630894829888 APTUS Medartis AG HWC 2026-06-01 07630894829895 APTUS Medartis AG HWC 2026-06-01 07630894829901 APTUS Medartis AG HWC 2026-06-01 07630894829918 APTUS Medartis AG HWC 2026-06-01 07630894829925 APTUS Medartis AG HWC 2026-06-01 07630894829932 APTUS Medartis AG HWC 2026-06-01 07630894829949 APTUS Medartis AG HWC 2026-06-01 07630894829956 APTUS Medartis AG HWC 2026-06-01 07630894829963 APTUS Medartis AG HWC 2026-06-01 07630894829970 APTUS Medartis AG HWC 2026-06-01 07630894829987 APTUS Medartis AG HWC 2026-06-01 07630894829994 APTUS Medartis AG HWC 2026-06-01