TOTAL MANDIBULAR SYSTEM 24-2555

GUDID 00841036061852

BIOMET MICROFIXATION, INC

Manual orthopaedic bender, reusable
Primary Device ID00841036061852
NIH Device Record Key8348f95d-36c2-498f-9a6e-4bf4163a22c9
Commercial Distribution StatusIn Commercial Distribution
Brand NameTOTAL MANDIBULAR SYSTEM
Version Model Number24-2555
Catalog Number24-2555
Company DUNS046189866
Company NameBIOMET MICROFIXATION, INC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(904)741-4400
EmailFXJAX-ORDERS@ZIMMERBIOMET.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS100841036061852 [Primary]

FDA Product Code

HXWBENDER

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00841036061852]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-01
Device Publish Date2018-08-30

On-Brand Devices [TOTAL MANDIBULAR SYSTEM]

0084103606682624-1136
0084103606277424-1135
0084103606268224-1130
0084103606255224-1131
0084103606143224-1138
0084103606508920-1300
0084103606357324-4545
0084103606356624-4544
0084103606346724-2550
0084103606323824-1302
0084103606284224-2556
0084103606241524-2400
0084103606185224-2555
0084103606114224-1308
0084103606082424-2115
0084103606081724-1306
0084103605927924-2050

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.