Columbus® CR DD NN1213

GUDID 04046964449994

ALL POLY TIBIA COLUMBUS CR DD T1 16MM

Aesculap AG

Cruciate-retaining total knee prosthesis

• Primary Device ID: 04046964449994
• NIH Device Record Key: 8dd38fa4-7789-4197-ac69-ab40f03b5aba
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Columbus® CR DD
• Version Model Number: NN1213
• Catalog Number: NN1213
• 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 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	04046964449994 [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: 2015-11-11

On-Brand Devices [Columbus® CR DD]

• 04046964451737: ALL POLY TIBIA COLUMBUS CR DD T5 12MM
• 04046964451706: ALL POLY TIBIA COLUMBUS CR DD T4 14MM
• 04046964451690: ALL POLY TIBIA COLUMBUS CR DD T4 12MM
• 04046964451683: ALL POLY TIBIA COLUMBUS CR DD T4 10MM
• 04046964451676: ALL POLY TIBIA COLUMBUS CR DD T3 16MM
• 04046964451669: ALL POLY TIBIA COLUMBUS CR DD T3 14MM
• 04046964451652: ALL POLY TIBIA COLUMBUS CR DD T3 12MM
• 04046964451614: ALL POLY TIBIA COLUMBUS CR DD T2 12MM
• 04046964449994: ALL POLY TIBIA COLUMBUS CR DD T1 16MM
• 04038653358991: COLUMBUS CR DD GLID.SURFACE T4/4+ 14MM
• 04038653358922: COLUMBUS CR DD GLID.SURFACE T2/2+ 16MM
• 04038653358878: COLUMBUS CR DD GLID.SURFACE T1/1+ 14MM