Primary Device ID | 04712602341769 |
NIH Device Record Key | be0a00f2-81c7-4fa7-b794-5b32d3e4440b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | U1 Hip System, Acetabular Cup |
Version Model Number | 1301-1056 |
Catalog Number | 1301-1056 |
Company DUNS | 656700556 |
Company Name | UNITED ORTHOPEDIC CORP. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +886229294567 |
service@uoc.com.tw |
Outer Diameter | 56 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04712602341769 [Primary] |
LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-08-02 |
Device Publish Date | 2015-10-24 |
04712602341790 | U1 Acetabular cup,62mm |
04712602341783 | U1 Acetabular cup,60mm |
04712602341776 | U1 Acetabular cup,58mm |
04712602341769 | U1 Acetabular cup,56mm |
04712602341752 | U1 Acetabular cup,54mm |
04712602341745 | U1 Acetabular cup,52mm |
04712602341738 | U1 Acetabular cup,50mm |
04712602341721 | U1 Acetabular cup,48mm |
04712602341714 | U1 Acetabular cup,46mm |
04712602341707 | U1 Acetabular cup,44mm |