OMNICHROMA FLOW

GUDID 04548190102242

Dental composite resin

Primary Device ID	04548190102242
NIH Device Record Key	16f6af39-37e6-42e4-b17f-1281d62f4ee6
Commercial Distribution Status	In Commercial Distribution
Brand Name	OMNICHROMA FLOW
Version Model Number	10224
Company DUNS	693552176
Company Name	TOKUYAMA DENTAL CORPORATION
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	true
Single Use	false
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

Device Issuing Agency	Device ID
GS1	04548190102242 [Primary]

EBF	Material, Tooth Shade, Resin

Steralize Prior To Use	false
Device Is Sterile	false

04548190102204	SYRINGE
04548190102242	SYRINGE SAMPLE KIT

Mark Image Registration \| Serial	Company Trademark Application Date
OMNICHROMA FLOW 79275695 not registered Live/Pending	TOKUYAMA CORPORATION 2019-09-17