LEVÓ DUAL MOTION BASE, REFURBISHED 7887-010R

GUDID 00842430108419

MIZUHO ORTHOPEDIC SYSTEMS, INC.

Head/neck procedure positioner
Primary Device ID00842430108419
NIH Device Record Key2728104b-3c72-4de7-8ebf-63e99d39111c
Commercial Distribution StatusIn Commercial Distribution
Brand NameLEVÓ DUAL MOTION BASE, REFURBISHED
Version Model Number7887-010R
Catalog Number7887-010R
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

Operating and Storage Conditions

Storage Environment Atmospheric PressureBetween 75 KiloPascal and 105 KiloPascal
Storage Environment Atmospheric PressureBetween 75 KiloPascal and 105 KiloPascal
Storage Environment Atmospheric PressureBetween 75 KiloPascal and 105 KiloPascal

Device Identifiers

Device Issuing AgencyDevice ID
GS100842430108419 [Primary]

FDA Product Code

JEATable, Surgical With Orthopedic Accessories, Ac-Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-11-12
Device Publish Date2018-10-12

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