PRK PERINEAL POST 5848-223

GUDID 00842430113802

MIZUHO ORTHOPEDIC SYSTEMS, INC.

Surgical counter-traction post Surgical counter-traction post Surgical counter-traction post Surgical counter-traction post Surgical counter-traction post Surgical counter-traction post Surgical counter-traction post Surgical counter-traction post Surgical counter-traction post Surgical counter-traction post Surgical counter-traction post Surgical counter-traction post Surgical counter-traction post Surgical counter-traction post
Primary Device ID00842430113802
NIH Device Record Key5e8b8cc5-b36d-47ce-8387-de1f6225ecc2
Commercial Distribution StatusIn Commercial Distribution
Brand NamePRK PERINEAL POST
Version Model Number5848-223
Catalog Number5848-223
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100842430113802 [Primary]
GS100842430113802 [Primary]
GS100842430113802 [Primary]
GS100842430113802 [Primary]
GS100842430113802 [Primary]
GS100842430113802 [Primary]
GS100842430113802 [Primary]
GS100842430113802 [Primary]
GS100842430113802 [Primary]
GS100842430113802 [Primary]
GS100842430113802 [Primary]
GS100842430113802 [Primary]
GS100842430113802 [Primary]
GS100842430113802 [Primary]

FDA Product Code

JEATable, Surgical With Orthopedic Accessories, Ac-Powered
JEATable, Surgical With Orthopedic Accessories, Ac-Powered
JEATable, Surgical With Orthopedic Accessories, Ac-Powered
JEATable, Surgical With Orthopedic Accessories, Ac-Powered
JEATable, Surgical With Orthopedic Accessories, Ac-Powered
JEATable, Surgical With Orthopedic Accessories, Ac-Powered
JEATable, Surgical With Orthopedic Accessories, Ac-Powered
JEATable, Surgical With Orthopedic Accessories, Ac-Powered
JEATable, Surgical With Orthopedic Accessories, Ac-Powered
JEATable, Surgical With Orthopedic Accessories, Ac-Powered
JEATable, Surgical With Orthopedic Accessories, Ac-Powered
JEATable, Surgical With Orthopedic Accessories, Ac-Powered
JEATable, Surgical With Orthopedic Accessories, Ac-Powered
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 Date2020-09-16
Device Publish Date2020-09-08

On-Brand Devices [PRK PERINEAL POST]

008424301138025848-223
008424301137345847-320

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