Combined KIT

GUDID 08806169145390

Dental Implant Instrument KIT / Combined KIT

DENTIS CO. ,LTD

Dental implant kit Dental implant kit Dental implant kit Dental implant kit Dental implant kit Dental implant kit Dental implant kit Dental implant kit Dental implant kit Dental implant kit Dental implant kit Dental implant kit Dental implant kit Dental implant kit Dental implant kit Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable Dental/maxillofacial surgical procedure kit, non-medicated, reusable

Primary Device ID	08806169145390
NIH Device Record Key	0e7ffbdf-a2e4-4427-9f1e-3d4b729e6924
Commercial Distribution Status	In Commercial Distribution
Brand Name	Combined KIT
Version Model Number	DGCK
Company DUNS	694721181
Company Name	DENTIS 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	true
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	true
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08806169145390 [Primary]

FDA Product Code

NDP	Accessories, Implant, Dental, Endosseous