Maxso M200

GUDID 00628504370087

M200-M/QD, Beyes QD Backend, Triple Spray, Non-Optic

Beyes Dental Canada Inc

Dental power tool system handpiece, pneumatic
Primary Device ID00628504370087
NIH Device Record Keye7ec4787-6529-4d41-8bb7-c00644b4889c
Commercial Distribution StatusIn Commercial Distribution
Brand NameMaxso M200
Version Model NumberHP2015
Company DUNS244261462
Company NameBeyes Dental Canada Inc
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 Batchfalse
Serial Numbertrue
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
GS100628504370087 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

EFBHandpiece, Air-Powered, Dental

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00628504370087]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-04-22
Device Publish Date2019-04-12

On-Brand Devices [Maxso M200]

00628504370087M200-M/QD, Beyes QD Backend, Triple Spray, Non-Optic
00628504370063M200-M/M4, M4 Backend, Triple Spray, Non-Optic

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