Abutment Protector PMM 33

GUDID 07899995211613

MICRO Mini AbutmentMENT PROTECTOR

Sin Sistema de Implante Nacional S/A

Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use Dental implant suprastructure, temporary, preformed, single-use

Primary Device ID	07899995211613
NIH Device Record Key	31f74807-3e6c-4a8e-8037-65411c071971
Commercial Distribution Status	In Commercial Distribution
Brand Name	Abutment Protector
Version Model Number	PMM 33
Catalog Number	PMM 33
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	false
Device Combination Product	false
Single Use	true
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	07899995211613 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170392

FDA Product Code

NHA	Abutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Use	false
Device Is Sterile	true

Device Entry Metadata

Public Version Status	New
Device Record Status	Published
Public Version Number	1
Public Version Date	2021-02-18
Device Publish Date	2021-02-10

On-Brand Devices [Abutment Protector]

07899995268440	PROTECTOR ABUTMENT MINI Ø6.0
07899995211613	MICRO Mini AbutmentMENT PROTECTOR
07899995211606	PROTECTOR ABUTMENT MINI Ø5.0
07899995211088	ABUTMENT PROTECTOR STANDART Ø5.0
07899995211064	ABUTMENT PROTECTOR CONICAL Ø5.0