Primary Device ID | 04712602345989 |
NIH Device Record Key | f782f3f7-dd6a-476d-bcab-374e3888db9e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | UKNEE Tibial baseplate, grooved |
Version Model Number | 2201-3030 |
Catalog Number | 2201-3030 |
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 |
04712602346016 | UKNEE Tibial baseplate,grooved,#6,XX-large |
04712602346009 | UKNEE Tibial baseplate,grooved,#5,X-large |
04712602345996 | UKNEE Tibial baseplate,grooved,#4,large |
04712602345989 | UKNEE Tibial baseplate,grooved,#3,medium |
04712602345972 | UKNEE Tibial baseplate,grooved,#2,small |
04712602345965 | UKNEE Tibial baseplate,grooved,#1,X-small |