Omron Dual Head Stethoscope 412BLK

GUDID 00073796412036

Dual Head Stethoscope - Black

Omron Healthcare, Inc.

Mechanical stethoscope Mechanical stethoscope Mechanical stethoscope Mechanical stethoscope Mechanical stethoscope Mechanical stethoscope Mechanical stethoscope Mechanical stethoscope Mechanical stethoscope Mechanical stethoscope
Primary Device ID00073796412036
NIH Device Record Keyc0b080e2-448e-41fa-bc71-183f8523790d
Commercial Distribution StatusIn Commercial Distribution
Brand NameOmron Dual Head Stethoscope
Version Model Number412BLK
Catalog Number412BLK
Company DUNS054318779
Company NameOmron Healthcare, Inc.
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 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-Countertrue

Customer Support Contacts

Phone800-634-4350
Emailohiquality@omron.com
Phone800-634-4350
Emailohiquality@omron.com
Phone800-634-4350
Emailohiquality@omron.com
Phone800-634-4350
Emailohiquality@omron.com
Phone800-634-4350
Emailohiquality@omron.com
Phone800-634-4350
Emailohiquality@omron.com
Phone800-634-4350
Emailohiquality@omron.com
Phone800-634-4350
Emailohiquality@omron.com
Phone800-634-4350
Emailohiquality@omron.com
Phone800-634-4350
Emailohiquality@omron.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100073796412036 [Primary]

FDA Product Code

LDEStethoscope, Manual

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-07-21
Device Publish Date2020-07-13

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