FDA UDI In Commercial Distribution 🇺🇸 United States

Welch Allyn, Inc.

DI: 00732094315554 · Model: 901134 · WELCH ALLYN, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Welch Allyn, Inc.
Primary DI
00732094315554
Version / Model
901134
Catalog Number
UPGES9-B-SRVENT-A
Company Name
WELCH ALLYN, INC.
Labeler DUNS
198227881
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-25
Public Version
1
Public Version Date
2020-04-02
Public Version Status
New
Public Device Record Key
d45987f0-025f-4a76-baae-705c77f5867b

Device Description

Upgrade E-Scribe Enterprise Server from v8.x to v9.x. Included are upgrades for the initial two node-locked workstation licenses. No change to the SQL database (Access or Oracle). No change to options like Worklists, Advanced Workflow, or Analysis.

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
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
DPS Electrocardiograph

GMDN Terms

Code Name
44106 Patient health record information system application software

Identifiers

Type ID
Primary 00732094315554

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K930558 000