FDA UDI In Commercial Distribution 🇺🇸 United States

3M™ Littmann® Classic III™

DI: 00707387789718 · Model: 5839 · 3M COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
3M™ Littmann® Classic III™
Primary DI
00707387789718
Version / Model
5839
Catalog Number
5839
Company Name
3M COMPANY
Labeler DUNS
830016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-08-16
Public Version
1
Public Version Date
2021-08-24
Public Version Status
New
Public Device Record Key
4560688f-5936-4217-9881-0e38b04c6240

Device Description

3M™ Littmann® Classic III™ Monitoring Stethoscope, 5839, Lemon-Lime Tube

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LDE STETHOSCOPE, MANUAL

GMDN Terms

Code Name
13755 Mechanical stethoscope

Identifiers

Type ID
Package 50707387789713
Primary 00707387789718

Customer Contacts