FDA UDI Not in Commercial Distribution 🇺🇸 United States

Welch Allyn, Inc.

DI: 00732094239157 · 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
00732094239157
Version / Model
901071
Catalog Number
411251
Company Name
WELCH ALLYN, INC.
Labeler DUNS
198227881
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-05
Public Version
4
Public Version Date
2023-09-19
Public Version Status
Update
Public Device Record Key
24501dd4-6031-4dda-9fbc-9a924bcd9eaf
Distribution End Date
2023-09-18

Device Description

590 LARGE DLV ASSEMBLY

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
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
Package 00732094239140
Primary 00732094239157
Package 00732094236545
Package 00732094236347

Customer Contacts