Primary Device ID | 04712771485318 |
NIH Device Record Key | b4677b56-f15c-4bf9-8ab3-9ef6938fefb5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | XPE Patellar, On set, 3 pegs |
Version Model Number | 2403-3260 |
Catalog Number | 2403-3260 |
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 |
04712771485325 | XPE Patellar, On set, 3 pegs, E-Larger, ψ 44 mm |
04712771485318 | XPE Patellar, On set, 3 pegs, XX-Larger, ψ 41 mm |
04712771485301 | XPE Patellar, On set, 3 pegs, X-Larger, ψ 38 mm |
04712771485295 | XPE Patellar, On set, 3 pegs, Larger, ψ 35 mm |
04712771485288 | XPE Patellar, On set, 3 pegs, Medium,ψ 32 mm |
04712771485271 | XPE Patellar, On set, 3 pegs, Small, ψ 29 mm |
04712771485264 | XPE Patellar, On set, 3 pegs, X-Small, ψ 26 mm |