FDA UDI In Commercial Distribution 🇺🇸 United States

Welch Allyn, Inc.

DI: 00732094344035 · Model: 901026 · WELCH ALLYN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Welch Allyn, Inc.
Primary DI
00732094344035
Version / Model
901026
Catalog Number
71-PM3LXES
Company Name
WELCH ALLYN, INC.
Labeler DUNS
198227881
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-25
Public Version
1
Public Version Date
2023-09-04
Public Version Status
New
Public Device Record Key
cc68c9e0-a115-4e55-92cd-6ca85267a302

Device Description

Diagnostic Set w PO & MV for iEx soft

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
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
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
ERA OTOSCOPE

GMDN Terms

Code Name
45084 Ophthalmic/otologic diagnostic set

Identifiers

Type ID
Primary 00732094344035

Customer Contacts