Primary Device ID | 04046963810757 |
NIH Device Record Key | e93449c2-1c5e-4c5a-a6a1-fe5012fbdf5e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VEGA System® PS |
Version Model Number | NX105 |
Catalog Number | NX105 |
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 |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com | |
Phone | +1(800)282-9000 |
GUDID.BBMUS_Service@bbraun.com |
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 Issuing Agency | Device ID |
---|---|
GS1 | 04046963810757 [Primary] |
JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2024-11-20 |
Device Publish Date | 2015-09-24 |
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 |
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 |