UHR UH1-61-28

GUDID 07613327017410

Bipolar Component

Howmedica Osteonics Corp.

Femoral head bipolar component Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty Bipolar femoral head outer component, hemiarthroplasty
Primary Device ID07613327017410
NIH Device Record Keyd572943d-4cd3-46c2-97bb-843d7de94b20
Commercial Distribution StatusIn Commercial Distribution
Brand NameUHR
Version Model NumberUH1-61-28
Catalog NumberUH1-61-28
Company DUNS058311945
Company NameHowmedica Osteonics 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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter
Outer Diameter61 Millimeter
Lumen/Inner Diameter28 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS107613327017410 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWLProsthesis, hip, hemi-, femoral, metal

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-09-24

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