FDA UDI In Commercial Distribution 🇺🇸 United States

Welch Allyn, Inc.

DI: 00732094230482 · Model: 901001 · WELCH ALLYN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
25

Basic Information

Brand Name
Welch Allyn, Inc.
Primary DI
00732094230482
Version / Model
901001
Catalog Number
411511
Company Name
WELCH ALLYN, INC.
Labeler DUNS
198227881
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2018-03-01
Public Version
3
Public Version Date
2023-11-02
Public Version Status
Update
Public Device Record Key
8a0c0fc2-a4f4-456d-99c8-3b6f50bf02b2

Device Description

5MM TIPS WITH SLEEVE

Device Characteristics

Single Use
Yes
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
No
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
12849 Otoscope, direct

Identifiers

Type ID
Primary 00732094230482
Package 00732094144246
Unit of Use 00732094141993
Package 00732094107920

Customer Contacts