Cement restrictor, I type 1907-1012

GUDID 04711605569279

Cement restrictor, I type, 12C

UNITED ORTHOPEDIC CORP.

Metal-on-polyethylene total hip prosthesis
Primary Device ID04711605569279
NIH Device Record Key01fae8bc-6e92-4608-ae66-c945bca090ef
Commercial Distribution StatusIn Commercial Distribution
Brand NameCement restrictor, I type
Version Model Number1907-1012
Catalog Number1907-1012
Company DUNS656700556
Company NameUNITED ORTHOPEDIC CORP.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+886229294567
Emailservice@uoc.com.tw

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS104711605569279 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWYProsthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-09-10
Device Publish Date2018-08-08

On-Brand Devices [Cement restrictor, I type]

04711605569309Cement restrictor, I type, 18C
04711605569293Cement restrictor, I type, 16C
04711605569286Cement restrictor, I type, 14C
04711605569279Cement restrictor, I type, 12C
04711605569262Cement restrictor, I type, 10C
04711605569255Cement restrictor, I type, 8C

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