FDA UDI In Commercial Distribution 🇺🇸 United States

Welch Allyn, Inc.

DI: 00732094322569 · Model: 901058 · WELCH ALLYN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Welch Allyn, Inc.
Primary DI
00732094322569
Version / Model
901058
Catalog Number
71WT-R
Company Name
WELCH ALLYN, INC.
Labeler DUNS
198227881
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-11
Public Version
1
Public Version Date
2023-09-19
Public Version Status
New
Public Device Record Key
02b10fe2-8fff-412b-ac0e-229dc00edaf3

Device Description

REFURB CSM NIBP SpO2 SURETEMP

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
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
57960 Multiple physiological parameter spot-check system, clinical

Identifiers

Type ID
Package 00732094322576
Primary 00732094322569

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K142356 000