Primary Device ID | 04719872179016 |
NIH Device Record Key | e6c948c3-6c2b-4ea6-bd2d-ccaea1776310 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | U-Motion™ |
Version Model Number | 1203-2232 |
Catalog Number | 1203-2232 |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
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 | |
Phone | +886229294567 |
tw.service@unitedorthopedic.com | |
Phone | +886229294567 |
tw.service@unitedorthopedic.com | |
Phone | +886229294567 |
tw.service@unitedorthopedic.com | |
Phone | +886229294567 |
tw.service@unitedorthopedic.com | |
Phone | +886229294567 |
tw.service@unitedorthopedic.com | |
Phone | +886229294567 |
tw.service@unitedorthopedic.com | |
Phone | +886229294567 |
tw.service@unitedorthopedic.com | |
Phone | +886229294567 |
tw.service@unitedorthopedic.com | |
Phone | +886229294567 |
tw.service@unitedorthopedic.com | |
Phone | +886229294567 |
tw.service@unitedorthopedic.com | |
Phone | +886229294567 |
tw.service@unitedorthopedic.com | |
Phone | +886229294567 |
tw.service@unitedorthopedic.com | |
Phone | +886229294567 |
tw.service@unitedorthopedic.com | |
Phone | +886229294567 |
tw.service@unitedorthopedic.com | |
Phone | +886229294567 |
tw.service@unitedorthopedic.com |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04719872179016 [Primary] |
LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented |
MEH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04719872179016]
Moist Heat or Steam Sterilization
[04719872179016]
Moist Heat or Steam Sterilization
[04719872179016]
Moist Heat or Steam Sterilization
[04719872179016]
Moist Heat or Steam Sterilization
[04719872179016]
Moist Heat or Steam Sterilization
[04719872179016]
Moist Heat or Steam Sterilization
[04719872179016]
Moist Heat or Steam Sterilization
[04719872179016]
Moist Heat or Steam Sterilization
[04719872179016]
Moist Heat or Steam Sterilization
[04719872179016]
Moist Heat or Steam Sterilization
[04719872179016]
Moist Heat or Steam Sterilization
[04719872179016]
Moist Heat or Steam Sterilization
[04719872179016]
Moist Heat or Steam Sterilization
[04719872179016]
Moist Heat or Steam Sterilization
[04719872179016]
Moist Heat or Steam Sterilization
[04719872179016]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2019-02-07 |
Device Publish Date | 2017-07-14 |
04719872179221 | Universal handle |
04719872179030 | Ceramic Femoral Head Trial, φ32mm, L |
04719872179023 | Ceramic Femoral Head Trial, φ28mm, L |
04719872179016 | Ceramic Femoral Head Trial, φ32mm, M |
04719872179009 | Ceramic Femoral Head Trial, φ28mm, M |
04719872178996 | Ceramic Femoral Head Trial, φ32mm, S |
04719872178989 | Ceramic Femoral Head Trial, φ28mm, S |
04719872173861 | Universal handle |
04719872173748 | Size plate, U-Motion |
04719872173731 | Liner impactor, 36mm |
04719872173724 | Liner impactor, 32mm |
04719872173717 | Liner impactor, 26mm |
04719872173700 | Femoral head impactor, 36mm |
04719872173694 | Ceramic head impactor, 36mm |
04719872173687 | Femoral head impactor, 32mm |
04719872173670 | Ceramic head impactor, 32mm |
04719872173663 | Femoral head impactor, 28mm |
04719872173656 | Ceramic head impactor, 28mm |
04719872173649 | Femoral head impactor, 26mm |
04719872173632 | Femoral head impactor, 22mm |
04719872173588 | Universal handle |