CODMAN MALIS 802943

GUDID 10886704039020

CODMAN MALIS Non Stick Mirror Finish Bayonet Bipolar Forceps 8 3/4 Inches (22.2cm) 0.4mm Angle down Tip

Cerenovus, Inc.

Open-surgery electrosurgical handpiece/electrode, bipolar, reusable

Primary Device ID	10886704039020
NIH Device Record Key	bd82392f-a803-48ce-8d34-d671707240f9
Commercial Distribution Discontinuation	2017-09-28
Commercial Distribution Status	Not in Commercial Distribution
Brand Name	CODMAN MALIS
Version Model Number	80-2943
Catalog Number	802943
Company DUNS	607846297
Company Name	Cerenovus, Inc.
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	false
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
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

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10886704039020 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K963499

FDA Product Code

GEI	ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES