MAXO2+

GUDID 00817770020677

MaxO2+A Analyzer with Adapter

MAXTEC, LLC

Respiratory oxygen monitor, line-powered
Primary Device ID00817770020677
NIH Device Record Keyfccca43f-7f28-4c7e-95e0-c222c47f9d25
Commercial Distribution Discontinuation2019-05-06
Commercial Distribution StatusNot in Commercial Distribution
Brand NameMAXO2+
Version Model NumberR217P62-004
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 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
GS100817770020677 [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 Number5
Public Version Date2019-05-07
Device Publish Date2016-09-26

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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