Primary Device ID | 04038653351701 |
NIH Device Record Key | 2154dc83-cbaf-4449-bebd-3235eca08b0b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Columbus® CR/PS |
Version Model Number | NN071K |
Catalog Number | NN071K |
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(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 | |
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 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 | 04038653351701 [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 | 2019-12-11 |
Device Publish Date | 2015-09-24 |
04038653445165 | COLUMBUS CR/PS TIB.PLATEAU CEMENTED T0 |
04038653445110 | COLUMBUS CR/PS TIB.PLATEAU CEMENTED T0+ |
04038653351787 | COLUMBUS CR/PS TIB.PLATEAU CEMENTED T5 |
04038653351770 | COLUMBUS CR/PS TIB.PLATEAU CEMENTED T4+ |
04038653351763 | COLUMBUS CR/PS TIB.PLATEAU CEMENTED T4 |
04038653351756 | COLUMBUS CR/PS TIB.PLATEAU CEMENTED T3+ |
04038653351749 | COLUMBUS CR/PS TIB.PLATEAU CEMENTED T3 |
04038653351732 | COLUMBUS CR/PS TIB.PLATEAU CEMENTED T2+ |
04038653351725 | COLUMBUS CR/PS TIB.PLATEAU CEMENTED T2 |
04038653351718 | COLUMBUS CR/PS TIB.PLATEAU CEMENTED T1+ |
04038653351701 | COLUMBUS CR/PS TIB.PLATEAU CEMENTED T1 |
04038653351824 | COLUMBUS CR/PS TIB.PLAT.PLASMAPORE T2+ |