| Primary Device ID | 04719886903218 |
| NIH Device Record Key | 9f67c062-1410-4839-b6a0-e1c3600dd2f3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DA Power Hook |
| Version Model Number | 9909-8501 |
| Catalog Number | 9909-8501 |
| 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 |
| 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 | |
| Phone | +886229294567 |
| tw.service@unitedorthopedic.com | |
| Phone | +886229294567 |
| tw.service@unitedorthopedic.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04719886903218 [Primary] |
| LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04719886903218]
Moist Heat or Steam Sterilization
[04719886903218]
Moist Heat or Steam Sterilization
[04719886903218]
Moist Heat or Steam Sterilization
[04719886903218]
Moist Heat or Steam Sterilization
[04719886903218]
Moist Heat or Steam Sterilization
[04719886903218]
Moist Heat or Steam Sterilization
[04719886903218]
Moist Heat or Steam Sterilization
[04719886903218]
Moist Heat or Steam Sterilization
[04719886903218]
Moist Heat or Steam Sterilization
[04719886903218]
Moist Heat or Steam Sterilization
[04719886903218]
Moist Heat or Steam Sterilization
[04719886903218]
Moist Heat or Steam Sterilization
[04719886903218]
Moist Heat or Steam Sterilization
[04719886903218]
Moist Heat or Steam Sterilization
[04719886903218]
Moist Heat or Steam Sterilization
[04719886903218]
Moist Heat or Steam Sterilization
[04719886903218]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-11-06 |
| Device Publish Date | 2024-10-29 |
| 04719886903218 - DA Power Hook | 2024-11-06DA Power hook case, #1 |
| 04719886903218 - DA Power Hook | 2024-11-06 DA Power hook case, #1 |
| 04719886903973 - U2 Total Knee System | 2024-11-06 PS Notch cutting jig, #1 |
| 04719886903980 - U2 Total Knee System | 2024-11-06 PS Notch cutting jig, #2 |
| 04719886903997 - U2 Total Knee System | 2024-11-06 PS Notch cutting jig, #5 |
| 04719886904000 - U2 Total Knee System | 2024-11-06 PS Notch cutting jig, #6 |
| 04719886904017 - U2 Total Knee System | 2024-11-06 PS Notch cutting jig, #7 |
| 04719886903546 - Resolve Modular Revision Stem | 2024-10-08 Proximal screw extractor, HEX 5 |
| 04719886903645 - U2 Total Knee System | 2024-10-08 Tibial cutting jig, open slot, 0°, left |