FDA UDI In Commercial Distribution 🇺🇸 United States

Welch Allyn, Inc.

DI: 00732094223897 · Model: 901039 · WELCH ALLYN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Welch Allyn, Inc.
Primary DI
00732094223897
Version / Model
901039
Catalog Number
5079-138
Company Name
WELCH ALLYN, INC.
Labeler DUNS
198227881
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-01-16
Public Version
1
Public Version Date
2020-01-24
Public Version Status
New
Public Device Record Key
0bbf61eb-c963-49ca-84b4-be4d9d5a1bee

Device Description

Welch Allyn Adult Professional Stethoscope, Plum

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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LDE STETHOSCOPE, MANUAL

GMDN Terms

Code Name
13755 Mechanical stethoscope

Identifiers

Type ID
Primary 00732094223897

Customer Contacts