CERABALT K30

GUDID 03760357970025

BERNARD CERVOS SOCIETE

Dental casting non-noble alloy
Primary Device ID03760357970025
NIH Device Record Key30ce9f27-994c-4199-aa68-1a971103d714
Commercial Distribution StatusIn Commercial Distribution
Brand NameCERABALT K30
Version Model NumberIngots 15x8 mm
Company DUNS346973803
Company NameBERNARD CERVOS SOCIETE
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 Usetrue
Lot Batchtrue
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
GS103760357970025 [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 Date2024-07-01
Device Publish Date2024-06-21

Devices Manufactured by BERNARD CERVOS SOCIETE

03760357972630 - NICRALLIUM N72024-07-08
03760357975075 - NICRALLIUM N42024-07-08
03760357975082 - NICRALLIUM N42024-07-08
03760357975099 - NICRALLIUM N42024-07-08
03760357970025 - CERABALT K302024-07-01
03760357970025 - CERABALT K302024-07-01
03760357970049 - NICRALLIUM N22024-07-01
03760357970063 - CERINOX C102024-07-01
03760357970186 - CERABALT K402024-07-01

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