RootEX standard 0.8 (sample)

GUDID 07630049901391

Endodontic instrument kit for root tip extraction

Diaswiss SA

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Primary Device ID	07630049901391
NIH Device Record Key	67c79de3-e65e-44a8-ab89-b5e4248918a5
Commercial Distribution Status	In Commercial Distribution
Brand Name	RootEX standard 0.8 (sample)
Version Model Number	935L.Set008-sam
Company DUNS	480296552
Company Name	Diaswiss SA
Device Count	1
DM Exempt	true
Pre-market Exempt	true
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	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07630049901391 [Primary]

FDA Product Code

EKS	FILE, PULP CANAL, ENDODONTIC