LEG WEDGE FOAM PAD (PER PAIR) 5880-80

GUDID 00842430112164

MIZUHO ORTHOPEDIC SYSTEMS, INC.

Leg/knee cushion Leg/knee cushion Leg/knee cushion Leg/knee cushion Leg/knee cushion Leg/knee cushion Leg/knee cushion Leg/knee cushion Leg/knee cushion Leg/knee cushion Leg/knee cushion Leg/knee cushion Leg/knee cushion Leg/knee cushion Leg/knee cushion
Primary Device ID00842430112164
NIH Device Record Key1790d79f-ddec-4728-bbeb-48186faf6c5e
Commercial Distribution StatusIn Commercial Distribution
Brand NameLEG WEDGE FOAM PAD (PER PAIR)
Version Model Number5880-80
Catalog Number5880-80
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
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
GS100842430112164 [Primary]
GS100842430112164 [Primary]
GS100842430112164 [Primary]
GS100842430112164 [Primary]
GS100842430112164 [Primary]
GS100842430112164 [Primary]
GS100842430112164 [Primary]
GS100842430112164 [Primary]
GS100842430112164 [Primary]
GS100842430112164 [Primary]
GS100842430112164 [Primary]
GS100842430112164 [Primary]
GS100842430112164 [Primary]
GS100842430112164 [Primary]
GS100842430112164 [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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