FDA UDI In Commercial Distribution 🇺🇸 United States

Welch Allyn, Inc.

DI: 00732094335439 · Model: 901058 · WELCH ALLYN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
8
Pkg Device Count
1

Basic Information

Brand Name
Welch Allyn, Inc.
Primary DI
00732094335439
Version / Model
901058
Catalog Number
74RE
Company Name
WELCH ALLYN, INC.
Labeler DUNS
198227881
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-08-25
Public Version
1
Public Version Date
2021-09-02
Public Version Status
New
Public Device Record Key
b84d5dde-8e51-4a2d-834c-5b2506fbd338

Device Description

WFR CSM NIBP Mas RRp Braun Pro6000

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MWI Monitor, physiological, patient (without arrhythmia detection or alarms)

GMDN Terms

Code Name
57962 Prostate electrolytic therapy system

Identifiers

Type ID
Package 00732094335781
Primary 00732094335439
Package 00732094335828
Package 00732094335798
Package 00732094335804
Package 00732094335811
Package 00732094335774
Package 00732094335767

Customer Contacts