Primary Device ID | 04038653445738 |
NIH Device Record Key | 9479fa0b-27bc-425a-a9d8-0741fffea0d2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Columbus® |
Version Model Number | NN561K |
Catalog Number | NN561K |
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(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 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 |
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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 Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04038653445738 [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 | 4 |
Public Version Date | 2022-01-25 |
Device Publish Date | 2015-09-24 |
04038653424795 | COLUMBUS TIB.HEMI-SPACER T5 8MM RL/LM |
04038653424788 | COLUMBUS TIB.HEMI-SPACER T4/4+ 8MM RL/LM |
04038653424771 | COLUMBUS TIB.HEMI-SPACER T3/3+ 8MM RL/LM |
04038653424764 | COLUMBUS TIB.HEMI-SPACER T2/2+ 8MM RL/LM |
04038653424740 | COLUMBUS TIB.HEMI-SPACER T5 4MM RL/LM |
04038653424733 | COLUMBUS TIB.HEMI-SPACER T4/4+ 4MM RL/LM |
04038653424726 | COLUMBUS TIB.HEMI-SPACER T3/3+ 4MM RL/LM |
04038653424719 | COLUMBUS TIB.HEMI-SPACER T2/2+ 4MM RL/LM |
04038653424627 | COLUMBUS TIB.HEMI-SPACER T3/3+ 4MM RM/LL |
04038653445752 | COLUMBUS TIB.HEMI-SPACER T0/0+ 8MM RL/LM |
04038653445745 | COLUMBUS TIB.HEMI-SPACER T0/0+ 4MM RL/LM |
04038653424757 | COLUMBUS TIB.HEMI-SPACER T1/1+ 8MM RL/LM |
04038653424665 | COLUMBUS TIB.HEMI-SPACER T2/2+ 8MM RM/LL |
04038653424641 | COLUMBUS TIB.HEMI-SPACER T5 4MM RM/LL |
04038653424634 | COLUMBUS TIB.HEMI-SPACER T4/4+ 4MM RM/LL |
04038653424610 | COLUMBUS TIB.HEMI-SPACER T2/2+ 4MM RM/LL |
04038653424702 | COLUMBUS TIB.HEMI-SPACER T1/1+ 4MM RL/LM |
04038653424603 | COLUMBUS TIB.HEMI-SPACER T1/1+ 8MM RM/LL |
04038653445721 | COLUMBUS TIB.HEMI-SPACER T0/0+ 4MM RM/LL |
04038653445738 | COLUMBUS TIB.HEMI-SPACER T0/0+ 8MM RM/LL |
04038653424696 | COLUMBUS TIB.HEMI-SPACER T5 8MM RM/LL |
04038653424689 | COLUMBUS TIB.HEMI-SPACER T4/4+ 8MM RM/LL |
04038653424672 | COLUMBUS TIB.HEMI-SPACER T3/3+ 8MM RM/LL |
04038653424597 | COLUMBUS TIB.HEMI-SPACER T1/1+ 4MM RM/LL |
04038653352609 | COLUMBUS PATELLA 3-PEGS P4 36X10MM |
04038653352593 | COLUMBUS PATELLA 3-PEGS P3 33X9MM |
04038653352586 | COLUMBUS PATELLA 3-PEGS P2 30X8MM |
04038653352579 | COLUMBUS PATELLA 3-PEGS P1 27X7MM |
04038653352265 | TIBIA EXTENSION STEM D14MM SHORT |