Columbus® CR/PS NN084K

GUDID 04038653351824

COLUMBUS CR/PS TIB.PLAT.PLASMAPORE T2+

Aesculap AG

Coated knee tibia prosthesis

• Primary Device ID: 04038653351824
• NIH Device Record Key: c9631aac-8a11-448d-a042-580c08f0ad00
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Columbus® CR/PS
• Version Model Number: NN084K
• Catalog Number: NN084K
• 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(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
• 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
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com

Device Dimensions

• 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 Identifiers

Device Issuing Agency	Device ID
GS1	04038653351824 [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: 2024-11-20
• Device Publish Date: 2015-09-24

On-Brand Devices [Columbus® CR/PS]

• 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+