STERNALOCK BLU SYSTEM SP-3055

GUDID 00841036169763

BIOMET MICROFIXATION, INC

Surgical screwdriver, reusable
Primary Device ID00841036169763
NIH Device Record Key02f5a759-9875-43a8-a267-ba021867162d
Commercial Distribution StatusIn Commercial Distribution
Brand NameSTERNALOCK BLU SYSTEM
Version Model NumberSP-3055
Catalog NumberSP-3055
Company DUNS046189866
Company NameBIOMET MICROFIXATION, INC
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 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
GS100841036169763 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HRSPLATE, FIXATION, BONE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00841036169763]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2018-10-05
Device Publish Date2015-10-11

On-Brand Devices [STERNALOCK BLU SYSTEM]

00841036216511SP-3323
00841036184476SP-3192
00841036184469SP-3191
00841036183141SP-3184
00841036183134SP-3185
00841036179519SP-3143
00841036170257SP-3052
00841036216498SP-3321
00841036203696SP-3261
00841036196059SP-3245
00841036182502SP-3188
00841036177072SP-3142
00841036170080SP-3040
00841036169848SP-3037
00841036169763SP-3055
00841036158651SP-2914
00841036158644SP-2913
00841036155391SP-2891
00888233017619SP-3192
00888233017596SP-3191

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