SURGICAL KIT EPIKUT LONG KCSEL 02

GUDID 07899995265067

SURGICAL KIT EPIKUT LONG

Sin Sistema de Implante Nacional S/A

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	07899995265067
NIH Device Record Key	535baeea-1ba5-4d88-b224-09f3c6cb6e27
Commercial Distribution Status	In Commercial Distribution
Brand Name	SURGICAL KIT EPIKUT LONG
Version Model Number	KCSEL 02
Catalog Number	KCSEL 02
Company DUNS	904569092
Company Name	Sin Sistema de Implante Nacional S/A
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	true
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	true
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 Identifiers

Device Issuing Agency	Device ID
GS1	07899995265067 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K222514

FDA Product Code

KCT	Sterilization Wrap Containers, Trays, Cassettes & Other Accessories