Primary Device ID | 04711605580687 |
NIH Device Record Key | e61f32ac-3101-43e5-80e0-7e5403c1bb82 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | U-Motion II PS Cup, no-hole, Ø50mm, ID36mm |
Version Model Number | 1306-3251 |
Catalog Number | 1306-3251 |
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 | 50 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04711605580687 [Primary] |
LZO | Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-08-07 |
Device Publish Date | 2018-04-19 |
04719886901658 - DA Power Hook | 2024-12-19 Power hook set |
04719886901665 - DA Power Hook | 2024-12-19 Mobile handle |
04719886901672 - DA Power Hook | 2024-12-19 Connector set |
04719886901689 - DA Power Hook | 2024-12-19 Extension bar |
04719886901696 - DA Power Hook | 2024-12-19 Side rail clamp, ACT-015, US |
04719886901702 - DA Power Hook | 2024-12-19 Femoral hook, 90°, left |
04719886901719 - DA Power Hook | 2024-12-19 Femoral hook, 90°, right |
04719886901726 - DA Power Hook | 2024-12-19 Femoral hook, 110°, left |