Titanium connecting bar, completely serrated, 230 014-10230

GUDID 04260029580938

MedXpert GmbH

Rib/rib cage internal fixation/bracing system bracing bar
Primary Device ID04260029580938
NIH Device Record Key0dd8b267-948c-49d1-856b-5a1f15103cb5
Commercial Distribution StatusIn Commercial Distribution
Brand NameTitanium connecting bar, completely serrated, 230
Version Model Number014-10230
Catalog Number014-10230
Company DUNS331019344
Company NameMedXpert GmbH
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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+4976345085630
Emailask-the-xpert@medXpert.de

Device Identifiers

Device Issuing AgencyDevice ID
GS104260029580938 [Primary]

FDA Product Code

HRSPlate, Fixation, Bone

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[04260029580938]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-01-05

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