Home GUDID H679601100380 LCP
Primary DI H679601100380
Brand LCP
Company Synthes GmbH
Model 60.110.038
Catalog number 60110038
Device description SCREW RACK FOR 2.4MM LCP DSTL RADIUS SYSTEM GRAPHIC CASE
Published 2018-07-18
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 FSM TRAY, SURGICAL, INSTRUMENT
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class FSM Tray, Surgical, Instrument General, Plastic Surgery 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 07611819326200 Direct Marking GS1 0 10886982242723 Primary GS1 0 H679601100380 Secondary HIBCC 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 07611819326200 07611819326200 7611819326200 10886982242723 10886982242723
GMDN Terms# Term, Definition table Term Definition Surgical instrument/implant rack A device designed as a small case, typically with a hinged lid that can be closed to protect the contents (i.e., surgical instruments and/or implantable devices such as plates or screws), and an integral rest(s) with grooves or notches in the upper edge so that the contents can be securely placed, protected, and organized. The lid or rest may be set at an angle to facilitate instrument/implant access during surgical procedures or sterilization. The device is typically be made of stainless steel or a suitable plastic material so that it can be sterilized. 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 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 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 00841731153258 ARTEMIS FUZE VILEX LLC FSM 2026-07-22 00841731153265 ARTEMIS TAKEDOWN VILEX LLC FSM 2026-07-22 B803PW12A0 ORTHOMED ORTHO-MED, INC. FSM 2026-07-22 B803PW14G0 ORTHOMED ORTHO-MED, INC. FSM 2026-07-22 B803PW18A0 ORTHOMED ORTHO-MED, INC. FSM 2026-07-22 B803PW20 ORTHOMED ORTHO-MED, INC. FSM 2026-07-22 B803PW22A0 ORTHOMED ORTHO-MED, INC. FSM 2026-07-22 B803PW26A0 ORTHOMED ORTHO-MED, INC. FSM 2026-07-22 B803PW30A0 ORTHOMED ORTHO-MED, INC. FSM 2026-07-22 B803PW32A0 ORTHOMED ORTHO-MED, INC. FSM 2026-07-22 B803PW40A0 ORTHOMED ORTHO-MED, INC. FSM 2026-07-22 B803PW6G0 ORTHOMED ORTHO-MED, INC. FSM 2026-07-22 00840606195737 Viaduct SPINAL ELEMENTS, INC. FSM 2026-07-20 00843059127478 Lattus TEDAN SURGICAL INNOVATIONS, L.L.C. FSM 2026-07-20 07613327602241 NA Stryker Leibinger GmbH & Co. KG FSM 2026-07-17 07613327602296 NA Stryker Leibinger GmbH & Co. KG FSM 2026-07-17 07613327602302 NA Stryker Leibinger GmbH & Co. KG FSM 2026-07-17 07613327602326 NA Stryker Leibinger GmbH & Co. KG FSM 2026-07-17 07613327602418 NA Stryker Leibinger GmbH & Co. KG FSM 2026-07-17 07613327663518 NA Stryker Leibinger GmbH & Co. KG FSM 2026-07-17 07613327663525 NA Stryker Leibinger GmbH & Co. KG FSM 2026-07-17 07613327663532 NA Stryker Leibinger GmbH & Co. KG FSM 2026-07-17 07613327663549 NA Stryker Leibinger GmbH & Co. KG FSM 2026-07-17 07613327663556 NA Stryker Leibinger GmbH & Co. KG FSM 2026-07-17 07613327663563 NA Stryker Leibinger GmbH & Co. KG FSM 2026-07-17 18257200028177 PHOENIX SFS Orthofix US LLC FSM 2026-07-17 18257200028207 PHOENIX SFS Orthofix US LLC FSM 2026-07-17 18257200028917 FIREBIRD SFS Orthofix US LLC FSM 2026-07-17 18257200028924 FIREBIRD SFS Orthofix US LLC FSM 2026-07-17 18257200028931 FIREBIRD SFS Orthofix US LLC FSM 2026-07-17
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