PREMIOtitan

GUDID D831TI18

PRIMOTEC LLC

Dental casting non-noble alloy
Primary Device IDD831TI18
NIH Device Record Keyf1a00bb2-232c-4a64-936b-707143157755
Commercial Distribution StatusIn Commercial Distribution
Brand NamePREMIOtitan
Version Model NumberTI-18
Company DUNS153454736
Company NamePRIMOTEC LLC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCD831TI18 [Primary]

FDA Product Code

EJHAlloy, Metal, Base

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-09-07
Device Publish Date2020-08-28

On-Brand Devices [PREMIOtitan]

D831TI20TI-20
D831TI18TI-18
D831TI15TI-15
D831TI135TI-13.5
D831TI12TI-12
D831TI10TI-10

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.