Patient Monitor

GUDID 06944413814752

Edan Instruments, Inc.

General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor General-purpose multi-parameter bedside monitor
Primary Device ID06944413814752
NIH Device Record Key9a74ecd9-0d90-441f-a6ec-5fc352014107
Commercial Distribution StatusIn Commercial Distribution
Brand NamePatient Monitor
Version Model NumberX8s
Company DUNS529173163
Company NameEdan Instruments, 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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS106944413814752 [Primary]

FDA Product Code

DQAOximeter

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-10-08
Device Publish Date2020-09-30

On-Brand Devices [Patient Monitor]

06944413808119PM-2000A+
06944413806726PM-2000M
06944413806696MM17
06944413806665PM-2000XL Plus
06944413806658PM-2000XL
06944413806641PM-2000XL Pro
06944413806634PM-2000A Pro
06944413806627PM-2000A
06944413802179iM20
06944413802162elite V6
06944413802155elite V5
06944413801844iM70
06944413801837iM60
06944413801707elite V8
06944413801646iM80
06944413801622iM50
06944413801615iM8B
06944413801608iM8A
06944413801592iM8
06944413800823M50
06944413800816M80
06944413810945X12
06944413810921X10
06944413810907X8
06944413814769X12s
06944413814752X8s
06944413814387X10s

Trademark Results [Patient Monitor]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PATIENT MONITOR
PATIENT MONITOR
74564296 1942340 Live/Registered
Brown, Frank L.
1994-08-22

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