Primary Device ID | 04038653352708 |
NIH Device Record Key | f12a53fa-c23b-4096-95bb-2f6e1c42a4ee |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Columbus® PS |
Version Model Number | NN523 |
Catalog Number | NN523 |
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 | 04038653352708 [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 |
04038653352135 | COLUMBUS PS FEMORAL COMP.CEMENTED F6L |
04038653352128 | COLUMBUS PS FEMORAL COMP.CEMENTED F5L |
04038653352111 | COLUMBUS PS FEMORAL COMP.CEMENTED F4L |
04038653352104 | COLUMBUS PS FEMORAL COMP.CEMENTED F3L |
04038653352098 | COLUMBUS PS FEMORAL COMP.CEMENTED F2L |
04038653352081 | COLUMBUS PS FEMORAL COMP.CEMENTED F1L |
04046963362089 | COLUMBUS PS NARROW FEMUR CEMENTED F6N R |
04046963362072 | COLUMBUS PS NARROW FEMUR CEMENTED F5N R |
04046963362065 | COLUMBUS PS NARROW FEMUR CEMENTED F4N R |
04046963362027 | COLUMBUS PS NARROW FEMUR CEMENTED F6N L |
04046963362010 | COLUMBUS PS NARROW FEMUR CEMENTED F5N L |
04046963362003 | COLUMBUS PS NARROW FEMUR CEMENTED F4N L |
04046963429348 | COLUMBUS PS NARROW FEMUR CEMENTED F3N R |
04046963429331 | COLUMBUS PS NARROW FEMUR CEMENTED F2N R |
04046963429294 | COLUMBUS PS NARROW FEMUR CEMENTED F3N L |
04046963429287 | COLUMBUS PS NARROW FEMUR CEMENTED F2N L |
04046963001520 | COLUMBUS PS FEMORAL COMP.CEMENTED F8R |
04046963001513 | COLUMBUS PS FEMORAL COMP.CEMENTED F8L |
04038653352210 | COLUMBUS PS FEMORAL COMP.CEMENTED F7R |
04038653352203 | COLUMBUS PS FEMORAL COMP.CEMENTED F6R |
04038653352197 | COLUMBUS PS FEMORAL COMP.CEMENTED F5R |
04038653352180 | COLUMBUS PS FEMORAL COMP.CEMENTED F4R |
04038653352173 | COLUMBUS PS FEMORAL COMP.CEMENTED F3R |
04038653352166 | COLUMBUS PS FEMORAL COMP.CEMENTED F2R |
04038653352159 | COLUMBUS PS FEMORAL COMP.CEMENTED F1R |
04038653352913 | COLUMBUS PS GLID.SURF.W/SCRW.T5 18MM |
04038653352869 | COLUMBUS PS GLID.SURF.W/SCRW.T5 10MM |
04038653352708 | COLUMBUS PS GLID.SURF.W/SCRW.T2/2+ 16MM |
04038653352692 | COLUMBUS PS GLID.SURF.W/SCRW.T2/2+ 14MM |