IU Fixture

GUDID 08800026100836

Dental implant system

Primary Device ID	08800026100836
NIH Device Record Key	7099413a-9fd6-4d0e-ba4e-068a4223117b
Commercial Distribution Status	In Commercial Distribution
Brand Name	IU Fixture
Version Model Number	FIU36100
Company DUNS	688857820
Company Name	WARANTEC.Co.,Ltd
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	true
Lot Batch	true
Serial Number	false
Manufacturing Date	true
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	08800026100836 [Primary]

DZE	Implant, Endosseous, Root-Form

Steralize Prior To Use	false
Device Is Sterile	true