PAD, MAIN TABLE, 5895 MAX ACCESS LAT 5895-7133

GUDID 00842430114526

MIZUHO ORTHOPEDIC SYSTEMS, INC.

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Primary Device ID00842430114526
NIH Device Record Keydee42968-a055-4785-9485-c3be8f0bd1af
Commercial Distribution StatusIn Commercial Distribution
Brand NamePAD, MAIN TABLE, 5895 MAX ACCESS LAT
Version Model Number5895-7133
Catalog Number5895-7133
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100842430114526 [Primary]
GS100842430114526 [Primary]
GS100842430114526 [Primary]
GS100842430114526 [Primary]
GS100842430114526 [Primary]
GS100842430114526 [Primary]
GS100842430114526 [Primary]
GS100842430114526 [Primary]
GS100842430114526 [Primary]
GS100842430114526 [Primary]
GS100842430114526 [Primary]
GS100842430114526 [Primary]
GS100842430114526 [Primary]
GS100842430114526 [Primary]
GS100842430114526 [Primary]

FDA Product Code

CCXSupport, Patient Position
CCXSupport, Patient Position
CCXSupport, Patient Position
CCXSupport, Patient Position
CCXSupport, Patient Position
CCXSupport, Patient Position
CCXSupport, Patient Position
CCXSupport, Patient Position
CCXSupport, Patient Position
CCXSupport, Patient Position
CCXSupport, Patient Position
CCXSupport, Patient Position
CCXSupport, Patient Position
CCXSupport, Patient Position
CCXSupport, Patient Position

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-01-13
Device Publish Date2021-01-05

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00842430113475 - SPLINT, BUCK'S TRAC, CONVOLUTED, SIZE M2021-01-20
00842430113529 - INFLATABLE CUFF/STRAP ASSEMBLY2021-01-20
00842430113536 - INFLATABLE MITT ASSY2021-01-20
00842430101236 - HANDPENDANT, RECONDITIONED,TRIOS, REFURB2021-01-13
00842430103513 - ASSEMBLY, CERVICAL LINKEAGE BAR, REFURB2021-01-13

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