FDA UDI In Commercial Distribution 🇺🇸 United States

Welch Allyn, Inc.

DI: 00732094214192 · Model: 901071 · WELCH ALLYN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
Welch Allyn, Inc.
Primary DI
00732094214192
Version / Model
901071
Catalog Number
410162
Company Name
WELCH ALLYN, INC.
Labeler DUNS
198227881
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-05
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
c1bc416f-26bb-439d-a7c9-46e898e56af6

Device Description

590 SMALL REFRESHED ASSEMBLY

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
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
HIB Speculum, vaginal, nonmetal

GMDN Terms

Code Name
37468 Vaginal speculum, single-use

Identifiers

Type ID
Primary 00732094214192
Package 00732094147766
Package 00732094143690
Package 00732094102277

Customer Contacts