FDA UDI In Commercial Distribution 🇺🇸 United States

Welch Allyn, Inc.

DI: 00732094339741 · Model: 901020 · WELCH ALLYN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Welch Allyn, Inc.
Primary DI
00732094339741
Version / Model
901020
Catalog Number
11840-BR
Company Name
WELCH ALLYN, INC.
Labeler DUNS
198227881
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-06
Public Version
1
Public Version Date
2021-05-14
Public Version Status
New
Public Device Record Key
217dfeef-32b1-41f6-9b82-84e2e39ee501

Device Description

WELCH ALLYN iEXAMINER BRAZIL LABELED

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HLI Ophthalmoscope, ac-powered

GMDN Terms

Code Name
45084 Ophthalmic/otologic diagnostic set

Identifiers

Type ID
Primary 00732094339741

Customer Contacts