Pusher 3 Leg 10x8

GUDID M209183110

BIOPRO, INC.

Orthopaedic prosthesis implantation instrument, reusable
Primary Device IDM209183110
NIH Device Record Key04e29240-5538-4420-9c06-14f75339ad25
Commercial Distribution StatusIn Commercial Distribution
Brand NamePusher 3 Leg 10x8
Version Model Number118311
Company DUNS618749857
Company NameBIOPRO, 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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM209183110 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[M209183110]

Moist Heat or Steam Sterilization


[M209183110]

Moist Heat or Steam Sterilization


[M209183110]

Moist Heat or Steam Sterilization


[M209183110]

Moist Heat or Steam Sterilization


[M209183110]

Moist Heat or Steam Sterilization


[M209183110]

Moist Heat or Steam Sterilization


[M209183110]

Moist Heat or Steam Sterilization


[M209183110]

Moist Heat or Steam Sterilization


[M209183110]

Moist Heat or Steam Sterilization


[M209183110]

Moist Heat or Steam Sterilization


[M209183110]

Moist Heat or Steam Sterilization


[M209183110]

Moist Heat or Steam Sterilization


[M209183110]

Moist Heat or Steam Sterilization


[M209183110]

Moist Heat or Steam Sterilization


[M209183110]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-05-09
Device Publish Date2019-05-01

On-Brand Devices [Pusher 3 Leg 10x8]

M209183110118311
0081001248407718311

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