FDA UDI In Commercial Distribution 🇺🇸 United States

Welch Allyn, Inc.

DI: 00732094335408 · Model: 901058 · WELCH ALLYN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
9
Pkg Device Count
1

Basic Information

Brand Name
Welch Allyn, Inc.
Primary DI
00732094335408
Version / Model
901058
Catalog Number
75RE
Company Name
WELCH ALLYN, INC.
Labeler DUNS
198227881
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-04-26
Public Version
1
Public Version Date
2023-05-04
Public Version Status
New
Public Device Record Key
c297c374-8171-4f04-a318-1565e3408c65

Device Description

WIFI 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
Primary 00732094335408
Package 00732094343397
Package 00732094335590
Package 00732094335606
Package 00732094335620
Package 00732094335644
Package 00732094335637
Package 00732094335613
Package 00732094335583

Customer Contacts