Guided Surgery 260-101-835

GUDID 00813110024541

Dental implant/prosthesis surgical procedure kit Dental implant/prosthesis surgical procedure kit

Primary Device ID	00813110024541
NIH Device Record Key	bf895ac9-15e4-4e7a-9b37-e24dd1964a1b
Commercial Distribution Status	In Commercial Distribution
Brand Name	Guided Surgery
Version Model Number	260-101-835
Catalog Number	260-101-835
Company DUNS	945015758
Company Name	BICON, LLC
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	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	00813110024541 [Primary]

NDP	Accessories, Implant, Dental, Endosseous

Steralize Prior To Use	true
Device Is Sterile	false

[00813110024541]

Moist Heat or Steam Sterilization

[00813110024541]

Moist Heat or Steam Sterilization