Drape Rod 6800-350

GUDID 00842430100147

MIZUHO ORTHOPEDIC SYSTEMS, INC.

Anaesthesia screen
Primary Device ID00842430100147
NIH Device Record Key2fb42604-8833-48b1-b855-e34a0837e7f3
Commercial Distribution StatusIn Commercial Distribution
Brand NameDrape Rod
Version Model Number6800-350
Catalog Number6800-350
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100842430100147 [Primary]

FDA Product Code

FQOTable, Operating-Room, Ac-Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-06-25
Device Publish Date2018-05-23

On-Brand Devices [Drape Rod]

008424301001476800-350
008424301145716300-421

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