Columbus® CR NN821K

GUDID 04046963429195

COLUMBUS CR NARROW FEMUR PLASMAP.F3N L

Aesculap AG

Coated knee femur prosthesis

• Primary Device ID: 04046963429195
• NIH Device Record Key: cf86a7a5-3342-4cb0-a61d-c5f31e52b9a2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Columbus® CR
• Version Model Number: NN821K
• Catalog Number: NN821K
• 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

Customer Support Contacts

• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
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• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04046963429195 [Primary]

FDA Product Code

• JWH: PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-07-30
• Device Publish Date: 2015-09-24

On-Brand Devices [Columbus® CR]

• 04038653351367: COLUMBUS CR FEMORAL COMP.CEMENTED F4L
• 04038653351343: COLUMBUS CR FEMORAL COMP.CEMENTED F2L
• 04038653351336: COLUMBUS CR FEMORAL COMP.CEMENTED F1L
• 04046963001506: COLUMBUS CR FEMORAL COMP.PLASMAPORE F8R
• 04046963001490: COLUMBUS CR FEMORAL COMP.PLASMAPORE F8L
• 04038653351688: COLUMBUS CR FEMORAL COMP.PLASMAPORE F6R
• 04038653351671: COLUMBUS CR FEMORAL COMP.PLASMAPORE F5R
• 04038653351664: COLUMBUS CR FEMORAL COMP.PLASMAPORE F4R
• 04038653351657: COLUMBUS CR FEMORAL COMP.PLASMAPORE F3R
• 04038653351640: COLUMBUS CR FEMORAL COMP.PLASMAPORE F2R
• 04038653351633: COLUMBUS CR FEMORAL COMP.PLASMAPORE F1R
• 04038653351626: COLUMBUS CR FEMORAL COMP.PLASMAPORE F7L
• 04038653351619: COLUMBUS CR FEMORAL COMP.PLASMAPORE F6L
• 04038653351602: COLUMBUS CR FEMORAL COMP.PLASMAPORE F5L
• 04038653351596: COLUMBUS CR FEMORAL COMP.PLASMAPORE F4L
• 04038653351589: COLUMBUS CR FEMORAL COMP.PLASMAPORE F3L
• 04038653351572: COLUMBUS CR FEMORAL COMP.PLASMAPORE F2L
• 04038653351565: COLUMBUS CR FEMORAL COMP.PLASMAPORE F1L
• 04038653351480: COLUMBUS CR FEMORAL COMP.CEMENTED F8R
• 04038653351473: COLUMBUS CR FEMORAL COMP.CEMENTED F7R
• 04038653351466: COLUMBUS CR FEMORAL COMP.CEMENTED F6R
• 04038653351459: COLUMBUS CR FEMORAL COMP.CEMENTED F5R
• 04038653351435: COLUMBUS CR FEMORAL COMP.CEMENTED F3R
• 04038653351428: COLUMBUS CR FEMORAL COMP.CEMENTED F2R
• 04038653351411: COLUMBUS CR FEMORAL COMP.CEMENTED F1R
• 04038653351404: COLUMBUS CR FEMORAL COMP.CEMENTED F8L
• 04038653351398: COLUMBUS CR FEMORAL COMP.CEMENTED F7L
• 04038653351381: COLUMBUS CR FEMORAL COMP.CEMENTED F6L
• 04038653351374: COLUMBUS CR FEMORAL COMP.CEMENTED F5L
• 04046963429140: COLUMBUS CR NARROW FEMUR CEMENTED F3N R
• 04046963429133: COLUMBUS CR NARROW FEMUR CEMENTED F2N R
• 04046963429126: COLUMBUS CR NARROW FEMUR CEMENTED F3N L
• 04046963429119: COLUMBUS CR NARROW FEMUR CEMENTED F2N L
• 04046963361860: COLUMBUS CR NARROW FEMUR CEMENTED F6N R
• 04046963361853: COLUMBUS CR NARROW FEMUR CEMENTED F5N R
• 04046963361846: COLUMBUS CR NARROW FEMUR CEMENTED F4N R
• 04046963361839: COLUMBUS CR NARROW FEMUR CEMENTED F6N L
• 04046963361822: COLUMBUS CR NARROW FEMUR CEMENTED F5N L
• 04046963361815: COLUMBUS CR NARROW FEMUR CEMENTED F4N L
• 04038653351442: COLUMBUS CR FEMORAL COMP.CEMENTED F4R
• 04046963429270: COLUMBUS CR NARROW FEMUR PLASMAP.F3N R
• 04046963429232: COLUMBUS CR NARROW FEMUR PLASMAP.F2N R
• 04046963429195: COLUMBUS CR NARROW FEMUR PLASMAP.F3N L
• 04046963429188: COLUMBUS CR NARROW FEMUR PLASMAP.F2N L
• 04046963361990: COLUMBUS CR NARROW FEMUR PLASMAP.F6N R
• 04046963361983: COLUMBUS CR NARROW FEMUR PLASMAP.F5N R
• 04046963361976: COLUMBUS CR NARROW FEMUR PLASMAP.F4N R
• 04046963361969: COLUMBUS CR NARROW FEMUR PLASMAP.F6N L
• 04046963361952: COLUMBUS CR NARROW FEMUR PLASMAP.F5N L
• 04046963361945: COLUMBUS CR NARROW FEMUR PLASMAP.F4N L