3M™ Littmann™ 8493

GUDID 50707387792430

3M™ Littmann™ Core Stethoscope, 8493, Black, EK

3M COMPANY

Electronic stethoscope
Primary Device ID50707387792430
NIH Device Record Key620dc003-0313-4677-a196-5787851f12e4
Commercial Distribution StatusIn Commercial Distribution
Brand Name3M™ Littmann™
Version Model Number8493
Catalog Number8493
Company DUNS830016148
Company Name3M COMPANY
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com
Phone+1(800)228-3957
Email3Mhealthcarecompliance@mmm.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100707387792435 [Primary]
GS150707387792430 [Package]
Contains: 00707387792435
Package: BOX [3 Units]
In Commercial Distribution

FDA Product Code

DQDSTETHOSCOPE, ELECTRONIC

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2024-08-07
Device Publish Date2022-12-08

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