Opti plus HD

GUDID 08800096901203

Intraoral camera

Primary Device ID	08800096901203
NIH Device Record Key	38e0cfae-adf9-4f8f-a9bf-65f2d4cd8501
Commercial Distribution Status	In Commercial Distribution
Brand Name	Opti plus HD
Version Model Number	Opti plus HD-Regular kit
Company DUNS	690440554
Company Name	Dentall co.,Ltd.
Device Count	1
DM Exempt	false
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	false
Serial Number	true
Manufacturing Date	true
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

Device Issuing Agency	Device ID
GS1	08800096901203 [Primary]

KQM	Camera, Surgical And Accessories

Steralize Prior To Use	false
Device Is Sterile	false

08800096901210	Intraoral Camera
08800096901203	Intraoral Camera