Primary Device ID | 04046963367589 |
NIH Device Record Key | 771bfc06-867f-41d7-a9a0-817b8fcb5938 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AS Columbus® |
Version Model Number | NN573Z |
Catalog Number | NN573Z |
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 | |
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 |
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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04046963367589 [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 |
04046963367527 | AS COLUMBUS TIB.HEMI-SP.T4/4+ 4MM RM/LL |
04046963367497 | AS COLUMBUS TIB.HEMI-SP.T1/1+ 4MM RM/LL |
04046963367725 | AS COLUMBUS TIB.HEMI-SP.T5 8MM RL/LM |
04046963367718 | AS COLUMBUS TIB.HEMI-SP.T4/4+ 8MM RL/LM |
04046963367701 | AS COLUMBUS TIB.HEMI-SP.T3/3+ 8MM RL/LM |
04046963367695 | AS COLUMBUS TIB.HEMI-SP.T2/2+ 8MM RL/LM |
04046963367657 | AS COLUMBUS TIB.HEMI-SP.T4/4+ 4MM RL/LM |
04046963367640 | AS COLUMBUS TIB.HEMI-SP.T3/3+ 4MM RL/LM |
04046963367633 | AS COLUMBUS TIB.HEMI-SP.T2/2+ 4MM RL/LM |
04046963367572 | AS COLUMBUS TIB.HEMI-SP.T3/3+ 8MM RM/LL |
04046963367510 | AS COLUMBUS TIB.HEMI-SP.T3/3+ 4MM RM/LL |
04046963367619 | AS COLUMBUS TIB.HEMI-SP.T1/1+ 4MM RL/LM |
04046963367596 | AS COLUMBUS TIB.HEMI-SP.T5 8MM RM/LL |
04046963367541 | AS COLUMBUS TIB.HEMI-SP.T0/0+ 8MM RM/LL |
04046963367480 | AS COLUMBUS TIB.HEMI-SP.T0/0+ 4MM RM/LL |
04046963367602 | AS COLUMBUS TIB.HEMI-SP.T0/0+ 4MM RL/LM |
04046963367558 | AS COLUMBUS TIB.HEMI-SP.T1/1+ 8MM RM/LL |
04046963367664 | AS COLUMBUS TIB.HEMI-SP.T5 4MM RL/LM |
04046963367688 | AS COLUMBUS TIB.HEMI-SP.T1/1+ 8MM RL/LM |
04046963367671 | AS COLUMBUS TIB.HEMI-SP.T0/0+ 8MM RL/LM |
04046963367589 | AS COLUMBUS TIB.HEMI-SP.T4/4+ 8MM RM/LL |
04046963367565 | AS COLUMBUS TIB.HEMI-SP.T2/2+ 8MM RM/LL |
04046963367534 | AS COLUMBUS TIB.HEMI-SP.T5 4MM RM/LL |
04046963367503 | AS COLUMBUS TIB.HEMI-SP.T2/2+ 4MM RM/LL |