CODMAN MALIS MODULE 1000 809104

GUDID 20886704039966

CODMAN MALIS MODULE 1000 Integrated Tubing and Unitized Bipolar Cord Set

CODMAN & SHURTLEFF, INC.

Electrical-only medical device connection cable, single-use

• Primary Device ID: 20886704039966
• NIH Device Record Key: 59a5781d-4e84-41f4-834d-d4f66e7243fc
• Commercial Distribution Discontinuation: 2017-09-28
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: CODMAN MALIS MODULE 1000
• Version Model Number: 80-9104
• Catalog Number: 809104
• Company DUNS: 607846297
• Company Name: CODMAN & SHURTLEFF, INC.
• Device Count: 10
• 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)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Waste Electrical and Electronic Equipment
• Special Storage Condition, Specify: Between 0 and 0 *Waste Electrical and Electronic Equipment
• Special Storage Condition, Specify: Between 0 and 0 *Waste Electrical and Electronic Equipment
• Special Storage Condition, Specify: Between 0 and 0 *Waste Electrical and Electronic Equipment
• Special Storage Condition, Specify: Between 0 and 0 *Waste Electrical and Electronic Equipment
• Special Storage Condition, Specify: Between 0 and 0 *Waste Electrical and Electronic Equipment
• Special Storage Condition, Specify: Between 0 and 0 *Waste Electrical and Electronic Equipment
• Special Storage Condition, Specify: Between 0 and 0 *Waste Electrical and Electronic Equipment
• Special Storage Condition, Specify: Between 0 and 0 *Waste Electrical and Electronic Equipment
• Special Storage Condition, Specify: Between 0 and 0 *Waste Electrical and Electronic Equipment
• Special Storage Condition, Specify: Between 0 and 0 *Waste Electrical and Electronic Equipment
• Special Storage Condition, Specify: Between 0 and 0 *Waste Electrical and Electronic Equipment
• Special Storage Condition, Specify: Between 0 and 0 *Waste Electrical and Electronic Equipment
• Special Storage Condition, Specify: Between 0 and 0 *Waste Electrical and Electronic Equipment
• Special Storage Condition, Specify: Between 0 and 0 *Waste Electrical and Electronic Equipment
• Special Storage Condition, Specify: Between 0 and 0 *Waste Electrical and Electronic Equipment
• Special Storage Condition, Specify: Between 0 and 0 *Waste Electrical and Electronic Equipment
• Special Storage Condition, Specify: Between 0 and 0 *Waste Electrical and Electronic Equipment
• Special Storage Condition, Specify: Between 0 and 0 *Waste Electrical and Electronic Equipment
• Special Storage Condition, Specify: Between 0 and 0 *Waste Electrical and Electronic Equipment

Device Identifiers

Device Issuing Agency	Device ID
GS1	10886704039969 [Unit of Use]
GS1	20886704039966 [Primary]

FDA Product Code

• GEI: ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-04-23
• Device Publish Date: 2016-06-30

On-Brand Devices [CODMAN MALIS MODULE 1000]

• 20886704039966: CODMAN MALIS MODULE 1000 Integrated Tubing and Unitized Bipolar Cord Set
• 20886704039942: CODMAN MALIS MODULE 1000 Integrated Tubing and Bipolar Cord Set