Columbus® REVISION F NR070K

GUDID 04046963338107

COLUMBUS REV F TIBIA OFFSET CEMENTED T0

Aesculap AG

Uncoated knee tibia prosthesis, metallic

• Primary Device ID: 04046963338107
• NIH Device Record Key: b2f6cec1-6d5a-48df-bf02-2c0c8a49f5c1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Columbus® REVISION F
• Version Model Number: NR070K
• Catalog Number: NR070K
• 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(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

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 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	04046963338107 [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: 2019-12-11
• Device Publish Date: 2015-09-24

On-Brand Devices [Columbus® REVISION F]

• 04046963337636: COLUMBUS REV F FEMUR CEMENTED F4R
• 04046963337612: COLUMBUS REV F FEMUR CEMENTED F2R
• 04046963337605: COLUMBUS REV F FEMUR CEMENTED F1R
• 04046963337582: COLUMBUS REV F FEMUR CEMENTED F7L
• 04046963337575: COLUMBUS REV F FEMUR CEMENTED F6L
• 04046963337568: COLUMBUS REV F FEMUR CEMENTED F5L
• 04046963337551: COLUMBUS REV F FEMUR CEMENTED F4L
• 04046963337544: COLUMBUS REV F FEMUR CEMENTED F3L
• 04046963337537: COLUMBUS REV F FEMUR CEMENTED F2L
• 04046963337520: COLUMBUS REV F FEMUR CEMENTED F1L
• 04046963338190: COLUMBUS REV F TIBIA OFFSET CEMENTED T5
• 04046963338183: COLUMBUS REV F TIBIA OFFSET CEMENTED T4+
• 04046963338176: COLUMBUS REV F TIBIA OFFSET CEMENTED T4
• 04046963338169: COLUMBUS REV F TIBIA OFFSET CEMENTED T3+
• 04046963338145: COLUMBUS REV F TIBIA OFFSET CEMENTED T2+
• 04046963338138: COLUMBUS REV F TIBIA OFFSET CEMENTED T2
• 04046963338121: COLUMBUS REV F TIBIA OFFSET CEMENTED T1+
• 04046963338114: COLUMBUS REV F TIBIA OFFSET CEMENTED T1
• 04046963338107: COLUMBUS REV F TIBIA OFFSET CEMENTED T0
• 04046963337667: COLUMBUS REV F FEMUR CEMENTED F7R
• 04046963337650: COLUMBUS REV F FEMUR CEMENTED F6R
• 04046963337643: COLUMBUS REV F FEMUR CEMENTED F5R
• 04046963337629: COLUMBUS REV F FEMUR CEMENTED F3R
• 04046963338152: COLUMBUS REV F TIBIA OFFSET CEMENTED T3
• 04046963338084: COLUMBUS REV F TIBIA OFFSET CEMENTED T0+
• 04046964010217: COLUMBUS REV F HC GLID.SURF.T5 24MM
• 04046964010057: COLUMBUS REV F HC GLID.SURF.T4/4+ 10MM
• 04046964010040: COLUMBUS REV F HC GLID.SURF.T3/3+ 28MM
• 04046964009990: COLUMBUS REV F HC GLID.SURF.T3/3+ 14MM
• 04046964009792: COLUMBUS REV F HC GLID.SURF.T5 18MM
• 04046964009709: COLUMBUS REV F HC GLID.SURF.T0/0+ 10MM
• 04046964009679: COLUMBUS REV F MC GLID.SURF.T5 24MM
• 04046964009594: COLUMBUS REV F MC GLID.SURF.T4/4+ 28MM
• 04046964009396: COLUMBUS REV F MC GLID.SURF.T1/1+ 18MM
• 04046964009372: COLUMBUS REV F MC GLID.SURF.T1/1+ 14MM
• 04046964009358: COLUMBUS REV F MC GLID.SURF.T1/1+ 10MM
• 04046964009273: COLUMBUS REV F MC GLID.SURF.T3/3+ 16MM
• 04046964009259: COLUMBUS REV F MC GLID.SURF.T3/3+ 12MM