Kerator Abutment

GUDID 08809488213115

Dental implant suprastructure, permanent, preformed

Primary Device ID	08809488213115
NIH Device Record Key	22a9d00a-6cec-40c4-ae35-f16397458cf2
Commercial Distribution Status	In Commercial Distribution
Brand Name	Kerator Abutment
Version Model Number	AR402
Company DUNS	688476027
Company Name	KJMEDITECH.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	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	08809488213115 [Primary]

NHA	Abutment, Implant, Dental, Endosseous

Steralize Prior To Use	true
Device Is Sterile	false

[08809488213115]

Moist Heat or Steam Sterilization