RevMed

Cefaly Technology SPRL 10601 Cefaly®

Company Name
Cefaly Technology SPRL
Catalog Number
10601

Description

Cefaly DUAL Enhanced is a newer version of Cefaly DUAL which is an FDA - cleared device Indications for Use:CEFALY DUAL Enhanced is for patients diagnosed by a physician with migraines per the FDA cleared indications for use.CEFALY DUAL Enhanced is indicated to be used for:The acute treatment of migraine with or without aura in patients 18 years of age or older.The preventative treatment of episodic migraine in patients 18 years of age or older.
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Additional Details

Device Identifier
05425018850273
Is RX
No
Is Over the Counter
Yes
Requires Sterilization
No
Is Sterile
No
Is Single Use
No

Barcode Mapping

Unit of MeasurementEachesGTIN
Each105425018850273