MAXO2+

GUDID 00817770020950

Analyzer with MicroMax BlenderBuddy 0-70 DISS

MAXTEC, LLC

Respiratory oxygen monitor, line-powered Respiratory oxygen monitor, line-powered
Primary Device ID00817770020950
NIH Device Record Key51b26342-7e11-475c-8420-963aebfff7ab
Commercial Distribution StatusIn Commercial Distribution
Brand NameMAXO2+
Version Model NumberR219P20-003
Company DUNS169911828
Company NameMAXTEC, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usefalse
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
GS100817770020950 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

CCLAnalyzer, Gas, Oxygen, Gaseous-Phase

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-01-14
Device Publish Date2016-09-28

On-Brand Devices [MAXO2+]

00817770020967Analyzer with MicroMax BlenderBuddy 0-15 0-3.5
00817770020950Analyzer with MicroMax BlenderBuddy 0-70 DISS
00817770020943Analyzer with Optiflow Jr.
00817770020677MaxO2+A Analyzer with Adapter
00817770020660Medical A International Analyzer

Trademark Results [MAXO2+]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MAXO2+
MAXO2+
78340964 3069090 Live/Registered
MAXTEC, LLC
2003-12-15

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