54-00348

GUDID 04546540237613

DYNAMIC MESH MALL. F. 2.0MM SCREWS

Stryker Leibinger GmbH & Co. KG

Craniofacial fixation plate, non-bioabsorbable
Primary Device ID04546540237613
NIH Device Record Key30903367-b606-4def-84d3-0c7a95dd542d
Commercial Distribution StatusIn Commercial Distribution
Version Model Number54-00348
Catalog Number54-00348
Company DUNS316153956
Company NameStryker Leibinger GmbH & Co. KG
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Length40 Millimeter
Length40 Millimeter
Length40 Millimeter
Length40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter
Device Size Text, specify0
Length4 Centimeter
Width4 Centimeter
Width40 Millimeter
Length40 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS104546540237613 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JEYPLATE, BONE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


[04546540237613]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-07-01
Device Publish Date2015-06-16

Devices Manufactured by Stryker Leibinger GmbH & Co. KG

07613252196259 - FLUOROMAP2025-02-05 FLUOROMAP 1.0 - SALES DEMO CD
07613252286578 - FLUOROMAP2025-02-05 FLUOROMAP 1.0 SOFTWARE
07613252286622 - FLUOROMAP2025-02-05 FLUOROMAP 1.0 - ENABLE
07613327401523 - NA2025-01-17 SternalPlate, Transverse, w/ bars
07613327401554 - NA2025-01-17 SternalPlate, T
07613327401561 - NA2025-01-17 SternalPlate, Transverse, w/ bars
07613327401738 - NA2025-01-17 SternalPlate, T
07613327634952 - NA2024-12-16 Drill for 6514-7-200 WL 16mm

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.