Primary Device ID | 04719886901672 |
NIH Device Record Key | df73cf3e-2250-4067-ae26-186dcce25272 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DA Power Hook |
Version Model Number | 9909-5606 |
Catalog Number | 9909-5606 |
Company DUNS | 656700556 |
Company Name | UNITED ORTHOPEDIC CORP. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 |
tw.service@unitedorthopedic.com | |
Phone | +886229294567 |
tw.service@unitedorthopedic.com | |
Phone | +886229294567 |
tw.service@unitedorthopedic.com | |
Phone | +886229294567 |
tw.service@unitedorthopedic.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04719886901672 [Primary] |
JEA | Table, Surgical With Orthopedic Accessories, Ac-Powered |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04719886901672]
Moist Heat or Steam Sterilization
[04719886901672]
Moist Heat or Steam Sterilization
[04719886901672]
Moist Heat or Steam Sterilization
[04719886901672]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-19 |
Device Publish Date | 2024-12-11 |
04719886903218 | DA Power hook case, #1 |
04719886901733 | Femoral hook, 110°, right |
04719886901726 | Femoral hook, 110°, left |
04719886901719 | Femoral hook, 90°, right |
04719886901702 | Femoral hook, 90°, left |
04719886901696 | Side rail clamp, ACT-015, US |
04719886901689 | Extension bar |
04719886901672 | Connector set |
04719886901665 | Mobile handle |
04719886901658 | Power hook set |