FDA UDI In Commercial Distribution 🇺🇸 United States

Welch Allyn, Inc.

DI: 00732094064216 · Model: 901061 · WELCH ALLYN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Welch Allyn, Inc.
Primary DI
00732094064216
Version / Model
901061
Catalog Number
802LT0N-0E0
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
9
Public Version Date
2022-06-28
Public Version Status
Update
Public Device Record Key
a54ae389-304c-47d1-81d2-3013e9ed78bf

Device Description

Welch Allyn Propaq LT Patient Monitor with 3/5-Lead ECG, AAMI Lead Color Coding,Nellcor SpO2, Smartcuf Motion-Tolerant NIBP, Pulse Rate, MAP, Impedance Pneumography Respiration, Full Patient Alarms and Trending, Adult/Pediatric/Neonate Patient Support, Shock Resistant; 220-240 V, 50- 60 Hz AC, Lead-Acid Battery; without charging cradle

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
36872 Multiple vital physiological parameter monitoring system, clinical

Identifiers

Type ID
Primary 00732094064216

Customer Contacts