Primary Device ID | 04712771480092 |
NIH Device Record Key | 9743b8ae-d566-464b-84ca-e6953a9a74d4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Tibial Baseplate, PSA type, Screw locking |
Version Model Number | 2203-5260 |
Catalog Number | 2203-5260 |
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 |
04712771480092 | Tibial Baseplate, PSA type, Screw locking, #6 |
04712771480085 | Tibial Baseplate, PSA type, Screw locking, #5 |
04712771480078 | Tibial Baseplate, PSA type, Screw locking, #4 |
04712771480061 | Tibial Baseplate, PSA type, Screw locking, #3 |
04712771480054 | Tibial Baseplate, PSA type, Screw locking, #2 |
04712771480047 | Tibial Baseplate, PSA type, Screw locking, #1 |