Hana/ProFx Femoral Hook Right 6850-918

GUDID 00842430106811

MIZUHO ORTHOPEDIC SYSTEMS, INC.

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Primary Device ID00842430106811
NIH Device Record Key430cc1e8-730f-4e7f-b768-1b9f0b82547c
Commercial Distribution StatusIn Commercial Distribution
Brand NameHana/ProFx Femoral Hook Right
Version Model Number6850-918
Catalog Number6850-918
Company DUNS084527241
Company NameMIZUHO ORTHOPEDIC SYSTEMS, 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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-800-777-4674
EmailCustServ@mizuhosi.com
Phone1-800-777-4674
EmailCustServ@mizuhosi.com
Phone1-800-777-4674
EmailCustServ@mizuhosi.com
Phone1-800-777-4674
EmailCustServ@mizuhosi.com
Phone1-800-777-4674
EmailCustServ@mizuhosi.com
Phone1-800-777-4674
EmailCustServ@mizuhosi.com
Phone1-800-777-4674
EmailCustServ@mizuhosi.com
Phone1-800-777-4674
EmailCustServ@mizuhosi.com
Phone1-800-777-4674
EmailCustServ@mizuhosi.com
Phone1-800-777-4674
EmailCustServ@mizuhosi.com
Phone1-800-777-4674
EmailCustServ@mizuhosi.com
Phone1-800-777-4674
EmailCustServ@mizuhosi.com
Phone1-800-777-4674
EmailCustServ@mizuhosi.com
Phone1-800-777-4674
EmailCustServ@mizuhosi.com
Phone1-800-777-4674
EmailCustServ@mizuhosi.com
Phone1-800-777-4674
EmailCustServ@mizuhosi.com
Phone1-800-777-4674
EmailCustServ@mizuhosi.com
Phone1-800-777-4674
EmailCustServ@mizuhosi.com
Phone1-800-777-4674
EmailCustServ@mizuhosi.com
Phone1-800-777-4674
EmailCustServ@mizuhosi.com
Phone1-800-777-4674
EmailCustServ@mizuhosi.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100842430106811 [Primary]

FDA Product Code

LHXTrousers, Anti-Shock
LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00842430106811]

Moist Heat or Steam Sterilization


[00842430106811]

Moist Heat or Steam Sterilization


[00842430106811]

Moist Heat or Steam Sterilization


[00842430106811]

Moist Heat or Steam Sterilization


[00842430106811]

Moist Heat or Steam Sterilization


[00842430106811]

Moist Heat or Steam Sterilization


[00842430106811]

Moist Heat or Steam Sterilization


[00842430106811]

Moist Heat or Steam Sterilization


[00842430106811]

Moist Heat or Steam Sterilization


[00842430106811]

Moist Heat or Steam Sterilization


[00842430106811]

Moist Heat or Steam Sterilization


[00842430106811]

Moist Heat or Steam Sterilization


[00842430106811]

Moist Heat or Steam Sterilization


[00842430106811]

Moist Heat or Steam Sterilization


[00842430106811]

Moist Heat or Steam Sterilization


[00842430106811]

Moist Heat or Steam Sterilization


[00842430106811]

Moist Heat or Steam Sterilization


[00842430106811]

Moist Heat or Steam Sterilization


[00842430106811]

Moist Heat or Steam Sterilization


[00842430106811]

Moist Heat or Steam Sterilization


[00842430106811]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-12-28
Device Publish Date2018-11-27

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00842430101328 - SPAR, LEG, LEFT, RADIOLUCENT, REFURBISHED2023-09-27
00842430101335 - SPAR ASSEMBLY, RIGHT, REFURBISHED2023-09-27
00842430101342 - SPAR ASSEMBLY, LEFT, REFURBISHED2023-09-27
00842430103414 - UPPER ARM SUPPORT & PAD, REFURBISHED2023-09-27

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