VEGA System® PS NX311
GUDID 04046964451867
ALL POLY TIBIA VEGA PS T1 12MM
Aesculap AG
Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis Posterior-stabilized total knee prosthesis| Primary Device ID | 04046964451867 |
| NIH Device Record Key | 038baa2c-4cea-4db0-a700-21ca5e51322a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VEGA System® PS |
| Version Model Number | NX311 |
| Catalog Number | NX311 |
| Company DUNS | 315018218 |
| Company Name | Aesculap AG |
| 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 |
Customer Support Contacts
| Phone | +1(888)229-3002 |
| setworld_orders@aesculap.com | |
| Phone | +1(888)229-3002 |
| setworld_orders@aesculap.com | |
| Phone | +1(888)229-3002 |
| setworld_orders@aesculap.com | |
| Phone | +1(888)229-3002 |
| setworld_orders@aesculap.com | |
| Phone | +1(888)229-3002 |
| setworld_orders@aesculap.com | |
| Phone | +1(888)229-3002 |
| setworld_orders@aesculap.com | |
| Phone | +1(888)229-3002 |
| setworld_orders@aesculap.com | |
| Phone | +1(888)229-3002 |
| setworld_orders@aesculap.com | |
| Phone | +1(888)229-3002 |
| setworld_orders@aesculap.com | |
| Phone | +1(888)229-3002 |
| setworld_orders@aesculap.com | |
| Phone | +1(888)229-3002 |
| setworld_orders@aesculap.com | |
| Phone | +1(888)229-3002 |
| setworld_orders@aesculap.com | |
| Phone | +1(888)229-3002 |
| setworld_orders@aesculap.com | |
| Phone | +1(888)229-3002 |
| setworld_orders@aesculap.com | |
| Phone | +1(888)229-3002 |
| setworld_orders@aesculap.com | |
| Phone | +1(888)229-3002 |
| setworld_orders@aesculap.com | |
| Phone | +1(888)229-3002 |
| setworld_orders@aesculap.com |
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04046964451867 [Primary] |
FDA Product Code
| JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2024-03-29 |
| Device Publish Date | 2015-11-11 |
On-Brand Devices [VEGA System® PS]
| 04046963810528 | VEGA PS TIBIAL PLATEAU CEMENTED T5 |
| 04046963810481 | VEGA PS TIBIAL PLATEAU CEMENTED T4 |
| 04046963810467 | VEGA PS TIBIAL PLATEAU CEMENTED T3+ |
| 04046963810429 | VEGA PS TIBIAL PLATEAU CEMENTED T2+ |
| 04046963810405 | VEGA PS TIBIAL PLATEAU CEMENTED T2 |
| 04046963810382 | VEGA PS TIBIAL PLATEAU CEMENTED T1+ |
| 04046963810368 | VEGA PS TIBIAL PLATEAU CEMENTED T1 |
| 04046963810344 | VEGA PS TIBIAL PLATEAU CEMENTED T0+ |
| 04046963810320 | VEGA PS TIBIAL PLATEAU CEMENTED T0 |
| 04046963810252 | VEGA PS FEMORAL COMPONENT CEMENTED F8R |
| 04046963810238 | VEGA PS FEMORAL COMPONENT CEMENTED F7R |
| 04046963810214 | VEGA PS FEMORAL COMPONENT CEMENTED F6R |
| 04046963810191 | VEGA PS FEMORAL COMPONENT CEMENTED F6N R |
| 04046963810177 | VEGA PS FEMORAL COMPONENT CEMENTED F5R |
| 04046963810153 | VEGA PS FEMORAL COMPONENT CEMENTED F5N R |
| 04046963810139 | VEGA PS FEMORAL COMPONENT CEMENTED F4R |
| 04046963810115 | VEGA PS FEMORAL COMPONENT CEMENTED F4N R |
| 04046963810092 | VEGA PS FEMORAL COMPONENT CEMENTED F3R |
| 04046963810078 | VEGA PS FEMORAL COMPONENT CEMENTED F3N R |
| 04046963810054 | VEGA PS FEMORAL COMPONENT CEMENTED F2R |
| 04046963810030 | VEGA PS FEMORAL COMPONENT CEMENTED F2N R |
| 04046963810016 | VEGA PS FEMORAL COMPONENT CEMENTED F1R |
| 04046963809997 | VEGA PS FEMORAL COMPONENT CEMENTED F8L |
| 04046963809973 | VEGA PS FEMORAL COMPONENT CEMENTED F7L |
| 04046963809959 | VEGA PS FEMORAL COMPONENT CEMENTED F6L |
| 04046963809935 | VEGA PS FEMORAL COMPONENT CEMENTED F6N L |
| 04046963809898 | VEGA PS FEMORAL COMPONENT CEMENTED F5N L |
| 04046963809874 | VEGA PS FEMORAL COMPONENT CEMENTED F4L |
| 04046963809850 | VEGA PS FEMORAL COMPONENT CEMENTED F4N L |
| 04046963809836 | VEGA PS FEMORAL COMPONENT CEMENTED F3L |
| 04046963809812 | VEGA PS FEMORAL COMPONENT CEMENTED F3N L |
| 04046963809799 | VEGA PS FEMORAL COMPONENT CEMENTED F2L |
| 04046963809775 | VEGA PS FEMORAL COMPONENT CEMENTED F2N L |
| 04046963809751 | VEGA PS FEMORAL COMPONENT CEMENTED F1L |
| 04046963810504 | VEGA PS TIBIAL PLATEAU CEMENTED T4+ |
| 04046963810443 | VEGA PS TIBIAL PLATEAU CEMENTED T3 |
| 04046963809911 | VEGA PS FEMORAL COMPONENT CEMENTED F5L |
| 04046964452048 | ALL POLY TIBIA VEGA PS T5 12MM |
| 04046964452031 | ALL POLY TIBIA VEGA PS T5 10MM |
| 04046964452024 | ALL POLY TIBIA VEGA PS T4 16MM |
| 04046964452017 | ALL POLY TIBIA VEGA PS T4 14MM |
| 04046964452000 | ALL POLY TIBIA VEGA PS T4 12MM |
| 04046964451911 | ALL POLY TIBIA VEGA PS T2 14MM |
| 04046964451904 | ALL POLY TIBIA VEGA PS T2 12MM |
| 04046964451898 | ALL POLY TIBIA VEGA PS T2 10MM |
| 04046964451881 | ALL POLY TIBIA VEGA PS T1 16MM |
| 04046964451874 | ALL POLY TIBIA VEGA PS T1 14MM |
| 04046964451867 | ALL POLY TIBIA VEGA PS T1 12MM |
| 04046964451850 | ALL POLY TIBIA VEGA PS T1 10MM |
| 04046964451843 | ALL POLY TIBIA VEGA PS T0 16MM |
Trademark Results [VEGA System]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VEGA SYSTEM 79079269 4054509 Live/Registered |
Aesculap AG 2009-12-18 |
 VEGA SYSTEM 75852519 2404071 Dead/Cancelled |
AESCULAP AG & CO. KG 1999-11-12 |
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