Magma NT 20019

GUDID D96720019

PREVEST DENPRO LIMITED

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Primary Device IDD96720019
NIH Device Record Key27d1c4a1-d5ff-4209-a592-d2f03d3af5ff
Commercial Distribution StatusIn Commercial Distribution
Brand NameMagma NT
Version Model NumberIntro Pack
Catalog Number20019
Company DUNS859546940
Company NamePREVEST DENPRO LIMITED
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCD96720019 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

EBFMaterial, Tooth Shade, Resin

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-05-01
Device Publish Date2024-04-23

On-Brand Devices [Magma NT]

D96720020Master Pack
D96720019Intro Pack
D96720003Unit Dose Compules
D96720001Refill Pack

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