Primary Device ID | 04719872149941 |
NIH Device Record Key | 71e4b4ef-2619-4950-8b5b-2d8f0aa45468 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | E-XPE Patellar, on set, 3 pegs |
Version Model Number | 2403-5270 |
Catalog Number | 2403-5270 |
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 |
04719872149941 | E-XPE Patellar, on set, 3 pegs, E-large, Ø44 mm |
04719872149934 | E-XPE Patellar, on set, 3 pegs, XX-large, Ø41 mm |
04719872149927 | E-XPE Patellar, on set, 3 pegs, X-large, Ø38 mm |
04719872149910 | E-XPE Patellar, on set, 3 pegs, large, Ø35 mm |
04719872149903 | E-XPE Patellar, on set, 3 pegs, medium,Ø32 mm |
04719872149897 | E-XPE Patellar, on set, 3 pegs, small, Ø29 mm |
04719872149880 | E-XPE Patellar, on set, 3 pegs, X-small, Ø26 mm |