Primary Device ID | 04711605584166 |
NIH Device Record Key | 916d3953-4a9e-4155-968e-a773807ed7a0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | U1 Total Hip System |
Version Model Number | 9201-7102 |
Catalog Number | 9201-7102 |
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 |
service@uoc.com.tw |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04711605584166 [Primary] |
HWT | Template |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04711605584166]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-01-04 |
Device Publish Date | 2017-06-23 |
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04711605584388 | Femoral sizer, anterior reference |
04711605584166 | Bipolar cap gauge |
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04711605583510 | Femoral A/P chamfer cutting guide, #3.5 |
04711605583503 | Femoral A/P chamfer cutting guide, #2.5 |
04711605583497 | Femoral A/P chamfer cutting guide, #1.5 |
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